Canonical Allele Identifier: CA1654866821

Gene: REV3L MFSD4B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111307294_111307295delinsAG , CM000668.2:g.111307294_111307295delinsAG	GRCh38
NC_000006.11:g.111628497_111628498delinsAG , CM000668.1:g.111628497_111628498delinsAG	GRCh37
NC_000006.10:g.111735190_111735191delinsAG	NCBI36
NG_053000.1:g.181421_181422delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368802.8:c.9252+66_9252+67delinsCT (REV3L) MANE Select	ENSP00000357792.3:n.9252+66_9252+67delinsCT
ENST00000666581.2:n.277+29136_277+29137delinsAG (MFSD4B)
ENST00000673245.1:n.273+11519_273+11520delinsAG (MFSD4B)
ENST00000673446.1:n.179+39457_179+39458delinsAG (MFSD4B)
ENST00000358835.7:c.9252+66_9252+67delinsCT (REV3L)	ENSP00000351697.3:n.9252+66_9252+67delinsCT
ENST00000368802.7:c.9252+66_9252+67delinsCT (REV3L)	ENSP00000357792.3:n.9252+66_9252+67delinsCT
ENST00000368805.5:c.9252+66_9252+67delinsCT (REV3L)	ENSP00000357795.1:n.9252+66_9252+67delinsCT
ENST00000422377.5:c.*9236+66_*9236+67delinsCT (REV3L)	ENSP00000393184.1:n.*9236+66_*9236+67delinsCT
ENST00000434009.5:c.*9343+66_*9343+67delinsCT (REV3L)	ENSP00000391605.1:n.*9343+66_*9343+67delinsCT
ENST00000435970.5:c.9018+66_9018+67delinsCT (REV3L)	ENSP00000402003.1:n.9018+66_9018+67delinsCT
ENST00000462119.5:n.1389+66_1389+67delinsCT (REV3L)
NM_001286431.1:c.9018+66_9018+67delinsCT (REV3L)	NP_001273360.1:n.9018+66_9018+67delinsCT
NM_001286432.1:c.9018+66_9018+67delinsCT (REV3L)	NP_001273361.1:n.9018+66_9018+67delinsCT
NM_002912.4:c.9252+66_9252+67delinsCT (REV3L)	NP_002903.3:n.9252+66_9252+67delinsCT
XM_006715543.2:c.9252+66_9252+67delinsCT (REV3L)	XP_006715606.1:n.9252+66_9252+67delinsCT
XM_006715544.2:c.9018+66_9018+67delinsCT (REV3L)	XP_006715607.1:n.9018+66_9018+67delinsCT
XM_011536028.1:c.9333+66_9333+67delinsCT (REV3L)	XP_011534330.1:n.9333+66_9333+67delinsCT
XM_011536029.1:c.9330+66_9330+67delinsCT (REV3L)	XP_011534331.1:n.9330+66_9330+67delinsCT
XM_011536030.1:c.9255+66_9255+67delinsCT (REV3L)	XP_011534332.1:n.9255+66_9255+67delinsCT
XM_011536031.1:c.9099+66_9099+67delinsCT (REV3L)	XP_011534333.1:n.9099+66_9099+67delinsCT
XM_011536032.1:c.9099+66_9099+67delinsCT (REV3L)	XP_011534334.1:n.9099+66_9099+67delinsCT
XR_942871.1:n.2045+29136_2045+29137delinsAG
XM_011536028.2:c.9333+66_9333+67delinsCT (REV3L)	XP_011534330.1:n.9333+66_9333+67delinsCT
XM_011536029.3:c.9330+66_9330+67delinsCT (REV3L)	XP_011534331.1:n.9330+66_9330+67delinsCT
XM_011536030.3:c.9255+66_9255+67delinsCT (REV3L)	XP_011534332.1:n.9255+66_9255+67delinsCT
XM_011536031.3:c.9099+66_9099+67delinsCT (REV3L)	XP_011534333.1:n.9099+66_9099+67delinsCT
XM_011536032.2:c.9099+66_9099+67delinsCT (REV3L)	XP_011534334.1:n.9099+66_9099+67delinsCT
XM_017011152.2:c.9096+66_9096+67delinsCT (REV3L)	XP_016866641.1:n.9096+66_9096+67delinsCT
XM_017011153.1:c.9096+66_9096+67delinsCT (REV3L)	XP_016866642.1:n.9096+66_9096+67delinsCT
XM_017011154.1:c.9096+66_9096+67delinsCT (REV3L)	XP_016866643.1:n.9096+66_9096+67delinsCT
XR_001743550.2:n.9438+66_9438+67delinsCT (REV3L)
XR_001743552.2:n.9360+66_9360+67delinsCT (REV3L)
XR_001743553.2:n.9756+66_9756+67delinsCT (REV3L)
XR_001743555.2:n.9678+66_9678+67delinsCT (REV3L)
XR_001743556.2:n.9485+66_9485+67delinsCT (REV3L)
XR_002956293.1:n.10696+66_10696+67delinsCT (REV3L)
NM_001286431.2:c.9018+66_9018+67delinsCT (REV3L)	NP_001273360.1:n.9018+66_9018+67delinsCT
NM_001372078.1:c.9252+66_9252+67delinsCT (REV3L) MANE Select	NP_001359007.1:n.9252+66_9252+67delinsCT
NM_001286432.2:c.9018+66_9018+67delinsCT (REV3L)	NP_001273361.1:n.9018+66_9018+67delinsCT
NM_002912.5:c.9252+66_9252+67delinsCT (REV3L)	NP_002903.3:n.9252+66_9252+67delinsCT