Canonical Allele Identifier: CA1654866757

Gene: REV3L MFSD4B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111307171_111307174delinsAAAT , CM000668.2:g.111307171_111307174delinsAAAT	GRCh38
NC_000006.11:g.111628374_111628377delinsAAAT , CM000668.1:g.111628374_111628377delinsAAAT	GRCh37
NC_000006.10:g.111735067_111735070delinsAAAT	NCBI36
NG_053000.1:g.181542_181545delinsATTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368802.8:c.9252+187_9252+190delinsATTT (REV3L) MANE Select	ENSP00000357792.3:n.9252+187_9252+190delinsATTT
ENST00000666581.2:n.277+29013_277+29016delinsAAAT (MFSD4B)
ENST00000673245.1:n.273+11396_273+11399delinsAAAT (MFSD4B)
ENST00000673446.1:n.179+39334_179+39337delinsAAAT (MFSD4B)
ENST00000358835.7:c.9252+187_9252+190delinsATTT (REV3L)	ENSP00000351697.3:n.9252+187_9252+190delinsATTT
ENST00000368802.7:c.9252+187_9252+190delinsATTT (REV3L)	ENSP00000357792.3:n.9252+187_9252+190delinsATTT
ENST00000368805.5:c.9252+187_9252+190delinsATTT (REV3L)	ENSP00000357795.1:n.9252+187_9252+190delinsATTT
ENST00000422377.5:c.*9236+187_*9236+190delinsATTT (REV3L)	ENSP00000393184.1:n.*9236+187_*9236+190delinsATTT
ENST00000434009.5:c.*9343+187_*9343+190delinsATTT (REV3L)	ENSP00000391605.1:n.*9343+187_*9343+190delinsATTT
ENST00000435970.5:c.9018+187_9018+190delinsATTT (REV3L)	ENSP00000402003.1:n.9018+187_9018+190delinsATTT
ENST00000462119.5:n.1389+187_1389+190delinsATTT (REV3L)
NM_001286431.1:c.9018+187_9018+190delinsATTT (REV3L)	NP_001273360.1:n.9018+187_9018+190delinsATTT
NM_001286432.1:c.9018+187_9018+190delinsATTT (REV3L)	NP_001273361.1:n.9018+187_9018+190delinsATTT
NM_002912.4:c.9252+187_9252+190delinsATTT (REV3L)	NP_002903.3:n.9252+187_9252+190delinsATTT
XM_006715543.2:c.9252+187_9252+190delinsATTT (REV3L)	XP_006715606.1:n.9252+187_9252+190delinsATTT
XM_006715544.2:c.9018+187_9018+190delinsATTT (REV3L)	XP_006715607.1:n.9018+187_9018+190delinsATTT
XM_011536028.1:c.9333+187_9333+190delinsATTT (REV3L)	XP_011534330.1:n.9333+187_9333+190delinsATTT
XM_011536029.1:c.9330+187_9330+190delinsATTT (REV3L)	XP_011534331.1:n.9330+187_9330+190delinsATTT
XM_011536030.1:c.9255+187_9255+190delinsATTT (REV3L)	XP_011534332.1:n.9255+187_9255+190delinsATTT
XM_011536031.1:c.9099+187_9099+190delinsATTT (REV3L)	XP_011534333.1:n.9099+187_9099+190delinsATTT
XM_011536032.1:c.9099+187_9099+190delinsATTT (REV3L)	XP_011534334.1:n.9099+187_9099+190delinsATTT
XR_942871.1:n.2045+29013_2045+29016delinsAAAT
XM_011536028.2:c.9333+187_9333+190delinsATTT (REV3L)	XP_011534330.1:n.9333+187_9333+190delinsATTT
XM_011536029.3:c.9330+187_9330+190delinsATTT (REV3L)	XP_011534331.1:n.9330+187_9330+190delinsATTT
XM_011536030.3:c.9255+187_9255+190delinsATTT (REV3L)	XP_011534332.1:n.9255+187_9255+190delinsATTT
XM_011536031.3:c.9099+187_9099+190delinsATTT (REV3L)	XP_011534333.1:n.9099+187_9099+190delinsATTT
XM_011536032.2:c.9099+187_9099+190delinsATTT (REV3L)	XP_011534334.1:n.9099+187_9099+190delinsATTT
XM_017011152.2:c.9096+187_9096+190delinsATTT (REV3L)	XP_016866641.1:n.9096+187_9096+190delinsATTT
XM_017011153.1:c.9096+187_9096+190delinsATTT (REV3L)	XP_016866642.1:n.9096+187_9096+190delinsATTT
XM_017011154.1:c.9096+187_9096+190delinsATTT (REV3L)	XP_016866643.1:n.9096+187_9096+190delinsATTT
XR_001743550.2:n.9438+187_9438+190delinsATTT (REV3L)
XR_001743552.2:n.9360+187_9360+190delinsATTT (REV3L)
XR_001743553.2:n.9756+187_9756+190delinsATTT (REV3L)
XR_001743555.2:n.9678+187_9678+190delinsATTT (REV3L)
XR_001743556.2:n.9485+187_9485+190delinsATTT (REV3L)
XR_002956293.1:n.10696+187_10696+190delinsATTT (REV3L)
NM_001286431.2:c.9018+187_9018+190delinsATTT (REV3L)	NP_001273360.1:n.9018+187_9018+190delinsATTT
NM_001372078.1:c.9252+187_9252+190delinsATTT (REV3L) MANE Select	NP_001359007.1:n.9252+187_9252+190delinsATTT
NM_001286432.2:c.9018+187_9018+190delinsATTT (REV3L)	NP_001273361.1:n.9018+187_9018+190delinsATTT
NM_002912.5:c.9252+187_9252+190delinsATTT (REV3L)	NP_002903.3:n.9252+187_9252+190delinsATTT