Canonical Allele Identifier: CA365254292

Gene: REV3L MFSD4B

Linked Data

• MyVariant Identifiers: chr6:g.111628629G>A (hg19) ; chr6:g.111307426G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111307426G>A , CM000668.2:g.111307426G>A	GRCh38
NC_000006.11:g.111628629G>A , CM000668.1:g.111628629G>A	GRCh37
NC_000006.10:g.111735322G>A	NCBI36
NG_053000.1:g.181290C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000368802.8:c.9187C>T (REV3L) MANE Select	ENSP00000357792.3:p.His3063Tyr
ENST00000666581.2:n.277+29268G>A (MFSD4B)
ENST00000673245.1:n.273+11651G>A (MFSD4B)
ENST00000673446.1:n.179+39589G>A (MFSD4B)
ENST00000358835.7:c.9187C>T (REV3L)	ENSP00000351697.3:p.His3063Tyr
ENST00000368802.7:c.9187C>T (REV3L)	ENSP00000357792.3:p.His3063Tyr
ENST00000368805.5:c.9187C>T (REV3L)	ENSP00000357795.1:p.His3063Tyr
ENST00000422377.5:c.*9171C>T (REV3L)	ENSP00000393184.1:n.*9171C>T
ENST00000434009.5:c.*9278C>T (REV3L)	ENSP00000391605.1:n.*9278C>T
ENST00000435970.5:c.8953C>T (REV3L)	ENSP00000402003.1:p.His2985Tyr
ENST00000462119.5:n.1324C>T (REV3L)
NM_001286431.1:c.8953C>T (REV3L)	NP_001273360.1:p.His2985Tyr
NM_001286432.1:c.8953C>T (REV3L)	NP_001273361.1:p.His2985Tyr
NM_002912.4:c.9187C>T (REV3L)	NP_002903.3:p.His3063Tyr
XM_006715543.2:c.9187C>T (REV3L)	XP_006715606.1:p.His3063Tyr
XM_006715544.2:c.8953C>T (REV3L)	XP_006715607.1:p.His2985Tyr
XM_011536028.1:c.9268C>T (REV3L)	XP_011534330.1:p.His3090Tyr
XM_011536029.1:c.9265C>T (REV3L)	XP_011534331.1:p.His3089Tyr
XM_011536030.1:c.9190C>T (REV3L)	XP_011534332.1:p.His3064Tyr
XM_011536031.1:c.9034C>T (REV3L)	XP_011534333.1:p.His3012Tyr
XM_011536032.1:c.9034C>T (REV3L)	XP_011534334.1:p.His3012Tyr
XR_942871.1:n.2045+29268G>A
XM_011536028.2:c.9268C>T (REV3L)	XP_011534330.1:p.His3090Tyr
XM_011536029.3:c.9265C>T (REV3L)	XP_011534331.1:p.His3089Tyr
XM_011536030.3:c.9190C>T (REV3L)	XP_011534332.1:p.His3064Tyr
XM_011536031.3:c.9034C>T (REV3L)	XP_011534333.1:p.His3012Tyr
XM_011536032.2:c.9034C>T (REV3L)	XP_011534334.1:p.His3012Tyr
XM_017011152.2:c.9031C>T (REV3L)	XP_016866641.1:p.His3011Tyr
XM_017011153.1:c.9031C>T (REV3L)	XP_016866642.1:p.His3011Tyr
XM_017011154.1:c.9031C>T (REV3L)	XP_016866643.1:p.His3011Tyr
XR_001743550.2:n.9373C>T (REV3L)
XR_001743552.2:n.9295C>T (REV3L)
XR_001743553.2:n.9691C>T (REV3L)
XR_001743555.2:n.9613C>T (REV3L)
XR_001743556.2:n.9420C>T (REV3L)
XR_002956293.1:n.10631C>T (REV3L)
NM_001286431.2:c.8953C>T (REV3L)	NP_001273360.1:p.His2985Tyr
NM_001372078.1:c.9187C>T (REV3L) MANE Select	NP_001359007.1:p.His3063Tyr
NM_001286432.2:c.8953C>T (REV3L)	NP_001273361.1:p.His2985Tyr
NM_002912.5:c.9187C>T (REV3L)	NP_002903.3:p.His3063Tyr