Canonical Allele Identifier: CA2838889293

Gene: RBFOX1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.7409229T>C , CM000678.2:g.7409229T>C	GRCh38
NC_000016.9:g.7459230T>C , CM000678.1:g.7459230T>C	GRCh37
NC_000016.8:g.7399231T>C	NCBI36
NG_011881.1:g.1395099T>C
NG_011881.2:g.2174478T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000705321.1:c.-34+80301T>C	ENSP00000516112.1:n.-34+80301T>C
ENST00000355637.9:c.87+76141T>C MANE Plus Clinical	ENSP00000347855.4:n.87+76141T>C
ENST00000550418.6:c.28-108918T>C MANE Select	ENSP00000450031.1:n.28-108918T>C
ENST00000641259.1:c.505-108918T>C	ENSP00000493041.1:n.505-108918T>C
ENST00000674626.1:c.-34+80301T>C	ENSP00000502217.1:n.-34+80301T>C
ENST00000675140.1:n.700-108918T>C
ENST00000675459.1:c.28-108918T>C	ENSP00000502616.1:n.28-108918T>C
ENST00000675562.1:c.102+104744T>C	ENSP00000501878.1:n.102+104744T>C
ENST00000675653.1:c.28-108918T>C	ENSP00000502718.1:n.28-108918T>C
ENST00000675842.1:c.28-108918T>C	ENSP00000501599.1:n.28-108918T>C
ENST00000311745.9:c.87+76141T>C	ENSP00000309117.5:n.87+76141T>C
ENST00000340209.8:c.42+76141T>C	ENSP00000344196.4:n.42+76141T>C
ENST00000355637.8:c.87+76141T>C	ENSP00000347855.4:n.87+76141T>C
ENST00000422070.8:c.157-108918T>C	ENSP00000391269.4:n.157-108918T>C
ENST00000436368.6:c.87+76141T>C	ENSP00000402745.2:n.87+76141T>C
ENST00000535565.6:c.136-108918T>C	ENSP00000438768.2:n.136-108918T>C
ENST00000547338.5:c.28-108918T>C	ENSP00000447717.1:n.28-108918T>C
ENST00000547372.5:c.157-108918T>C	ENSP00000446842.1:n.157-108918T>C
ENST00000547605.5:c.28-108918T>C	ENSP00000450402.1:n.28-108918T>C
ENST00000550418.5:c.28-108918T>C	ENSP00000450031.1:n.28-108918T>C
ENST00000551752.5:c.28-108918T>C	ENSP00000447281.1:n.28-108918T>C
ENST00000552089.5:c.136-108918T>C	ENSP00000448496.1:n.136-108918T>C
ENST00000553186.5:c.28-108918T>C	ENSP00000447753.1:n.28-108918T>C
ENST00000620507.4:c.42+76141T>C	ENSP00000484837.1:n.42+76141T>C
NM_001142333.1:c.28-108918T>C	NP_001135805.1:n.28-108918T>C
NM_001142334.1:c.28-108918T>C	NP_001135806.1:n.28-108918T>C
NM_001308117.1:c.157-108918T>C	NP_001295046.1:n.157-108918T>C
NM_018723.3:c.28-108918T>C	NP_061193.2:n.28-108918T>C
NM_145891.2:c.87+76141T>C	NP_665898.1:n.87+76141T>C
NM_145892.2:c.87+76141T>C	NP_665899.1:n.87+76141T>C
NM_145893.2:c.87+76141T>C	NP_665900.1:n.87+76141T>C
XM_005255379.2:c.157-108918T>C	XP_005255436.1:n.157-108918T>C
XM_005255380.2:c.136-108918T>C	XP_005255437.1:n.136-108918T>C
XM_005255381.2:c.102+104744T>C	XP_005255438.1:n.102+104744T>C
XM_005255382.2:c.87+76141T>C	XP_005255439.1:n.87+76141T>C
XM_005255384.2:c.28-108918T>C	XP_005255441.1:n.28-108918T>C
XM_005255385.3:c.28-108918T>C	XP_005255442.1:n.28-108918T>C
XM_005255386.2:c.102+104744T>C	XP_005255443.1:n.102+104744T>C
XM_005255387.2:c.87+76141T>C	XP_005255444.1:n.87+76141T>C
XM_005255390.2:c.28-108918T>C	XP_005255447.1:n.28-108918T>C
XM_005255391.2:c.28-108918T>C	XP_005255448.1:n.28-108918T>C
XM_005255393.2:c.87+76141T>C	XP_005255450.1:n.87+76141T>C
XM_005255394.3:c.87+76141T>C	XP_005255451.1:n.87+76141T>C
XM_011522544.1:c.505-108918T>C	XP_011520846.1:n.505-108918T>C
XM_011522546.1:c.87+76141T>C	XP_011520848.1:n.87+76141T>C
XM_011522547.1:c.87+76141T>C	XP_011520849.1:n.87+76141T>C
XM_011522548.1:c.87+76141T>C	XP_011520850.1:n.87+76141T>C
NM_001364800.1:c.28-108918T>C	NP_001351729.1:n.28-108918T>C
XM_005255386.4:c.102+104744T>C	XP_005255443.1:n.102+104744T>C
XM_005255387.4:c.87+76141T>C	XP_005255444.1:n.87+76141T>C
XM_005255390.4:c.28-108918T>C	XP_005255447.1:n.28-108918T>C
XM_005255391.4:c.28-108918T>C	XP_005255448.1:n.28-108918T>C
XM_005255394.4:c.87+76141T>C	XP_005255451.1:n.87+76141T>C
XM_011522546.2:c.87+76141T>C	XP_011520848.1:n.87+76141T>C
XM_011522547.2:c.87+76141T>C	XP_011520849.1:n.87+76141T>C
XM_011522548.2:c.87+76141T>C	XP_011520850.1:n.87+76141T>C
XM_017023318.2:c.625-108918T>C	XP_016878807.1:n.625-108918T>C
XM_017023319.2:c.625-108918T>C	XP_016878808.1:n.625-108918T>C
XM_017023320.2:c.157-108918T>C	XP_016878809.1:n.157-108918T>C
XM_017023321.2:c.136-108918T>C	XP_016878810.1:n.136-108918T>C
XM_017023322.2:c.136-108918T>C	XP_016878811.1:n.136-108918T>C
XM_017023323.2:c.102+104744T>C	XP_016878812.1:n.102+104744T>C
XM_017023324.2:c.157-108918T>C	XP_016878813.1:n.157-108918T>C
XM_017023326.2:c.28-108918T>C	XP_016878815.1:n.28-108918T>C
XM_017023327.1:c.102+104744T>C	XP_016878816.1:n.102+104744T>C
XM_017023328.2:c.157-108918T>C	XP_016878817.1:n.157-108918T>C
XM_017023329.2:c.157-108918T>C	XP_016878818.1:n.157-108918T>C
XM_017023330.1:c.136-108918T>C	XP_016878819.1:n.136-108918T>C
XM_017023332.1:c.102+104744T>C	XP_016878821.1:n.102+104744T>C
XM_017023333.1:c.28-108918T>C	XP_016878822.1:n.28-108918T>C
XM_017023334.1:c.102+104744T>C	XP_016878823.1:n.102+104744T>C
XM_017023335.2:c.28-108918T>C	XP_016878824.1:n.28-108918T>C
XM_017023336.1:c.28-108918T>C	XP_016878825.1:n.28-108918T>C
XM_017023337.1:c.102+104744T>C	XP_016878826.1:n.102+104744T>C
XM_017023338.1:c.28-108918T>C	XP_016878827.1:n.28-108918T>C
XM_017023340.1:c.28-108918T>C	XP_016878829.1:n.28-108918T>C
XM_017023341.2:c.28-108918T>C	XP_016878830.1:n.28-108918T>C
XM_017023342.1:c.28-108918T>C	XP_016878831.1:n.28-108918T>C
XM_024450303.1:c.586-108918T>C	XP_024306071.1:n.586-108918T>C
XM_024450304.1:c.136-108918T>C	XP_024306072.1:n.136-108918T>C
XM_024450305.1:c.136-108918T>C	XP_024306073.1:n.136-108918T>C
XM_024450306.1:c.87+76141T>C	XP_024306074.1:n.87+76141T>C
XM_024450307.1:c.28-108918T>C	XP_024306075.1:n.28-108918T>C
XM_024450308.1:c.102+104744T>C	XP_024306076.1:n.102+104744T>C
XM_024450309.1:c.157-108918T>C	XP_024306077.1:n.157-108918T>C
XM_024450310.1:c.157-108918T>C	XP_024306078.1:n.157-108918T>C
XM_024450311.1:c.136-108918T>C	XP_024306079.1:n.136-108918T>C
XM_024450312.1:c.136-108918T>C	XP_024306080.1:n.136-108918T>C
XM_024450313.1:c.136-108918T>C	XP_024306081.1:n.136-108918T>C
XM_024450314.1:c.157-108918T>C	XP_024306082.1:n.157-108918T>C
XM_024450316.1:c.28-108918T>C	XP_024306084.1:n.28-108918T>C
NM_001142333.2:c.28-108918T>C	NP_001135805.1:n.28-108918T>C
NM_001364800.2:c.28-108918T>C	NP_001351729.1:n.28-108918T>C
NM_018723.4:c.28-108918T>C MANE Select	NP_061193.2:n.28-108918T>C
NM_145891.3:c.87+76141T>C	NP_665898.1:n.87+76141T>C
NM_145892.3:c.87+76141T>C	NP_665899.1:n.87+76141T>C
NM_145893.3:c.87+76141T>C MANE Plus Clinical	NP_665900.1:n.87+76141T>C
NM_001142334.2:c.28-108918T>C	NP_001135806.1:n.28-108918T>C