Canonical Allele Identifier: CA3961086

Gene: REV3L MFSD4B

Linked Data

• dbSNP Id: rs766889673
• ExAC: 6:111628643 C / T
• gnomAD v2: 6-111628643-C-T
• gnomAD v3: 6-111307440-C-T
• gnomAD v4: 6-111307440-C-T
• COSMIC: COSM3857537 ; COSM3857538
• MyVariant Identifiers: chr6:g.111628643C>T (hg19) ; chr6:g.111307440C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111307440C>T , CM000668.2:g.111307440C>T	GRCh38
NC_000006.11:g.111628643C>T , CM000668.1:g.111628643C>T	GRCh37
NC_000006.10:g.111735336C>T	NCBI36
NG_053000.1:g.181276G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368802.8:c.9173G>A (REV3L) MANE Select	ENSP00000357792.3:p.Arg3058Gln
ENST00000666581.2:n.277+29282C>T (MFSD4B)
ENST00000673245.1:n.273+11665C>T (MFSD4B)
ENST00000673446.1:n.179+39603C>T (MFSD4B)
ENST00000358835.7:c.9173G>A (REV3L)	ENSP00000351697.3:p.Arg3058Gln
ENST00000368802.7:c.9173G>A (REV3L)	ENSP00000357792.3:p.Arg3058Gln
ENST00000368805.5:c.9173G>A (REV3L)	ENSP00000357795.1:p.Arg3058Gln
ENST00000422377.5:c.*9157G>A (REV3L)	ENSP00000393184.1:n.*9157G>A
ENST00000434009.5:c.*9264G>A (REV3L)	ENSP00000391605.1:n.*9264G>A
ENST00000435970.5:c.8939G>A (REV3L)	ENSP00000402003.1:p.Arg2980Gln
ENST00000462119.5:n.1310G>A (REV3L)
NM_001286431.1:c.8939G>A (REV3L)	NP_001273360.1:p.Arg2980Gln
NM_001286432.1:c.8939G>A (REV3L)	NP_001273361.1:p.Arg2980Gln
NM_002912.4:c.9173G>A (REV3L)	NP_002903.3:p.Arg3058Gln
XM_006715543.2:c.9173G>A (REV3L)	XP_006715606.1:p.Arg3058Gln
XM_006715544.2:c.8939G>A (REV3L)	XP_006715607.1:p.Arg2980Gln
XM_011536028.1:c.9254G>A (REV3L)	XP_011534330.1:p.Arg3085Gln
XM_011536029.1:c.9251G>A (REV3L)	XP_011534331.1:p.Arg3084Gln
XM_011536030.1:c.9176G>A (REV3L)	XP_011534332.1:p.Arg3059Gln
XM_011536031.1:c.9020G>A (REV3L)	XP_011534333.1:p.Arg3007Gln
XM_011536032.1:c.9020G>A (REV3L)	XP_011534334.1:p.Arg3007Gln
XR_942871.1:n.2045+29282C>T
XM_011536028.2:c.9254G>A (REV3L)	XP_011534330.1:p.Arg3085Gln
XM_011536029.3:c.9251G>A (REV3L)	XP_011534331.1:p.Arg3084Gln
XM_011536030.3:c.9176G>A (REV3L)	XP_011534332.1:p.Arg3059Gln
XM_011536031.3:c.9020G>A (REV3L)	XP_011534333.1:p.Arg3007Gln
XM_011536032.2:c.9020G>A (REV3L)	XP_011534334.1:p.Arg3007Gln
XM_017011152.2:c.9017G>A (REV3L)	XP_016866641.1:p.Arg3006Gln
XM_017011153.1:c.9017G>A (REV3L)	XP_016866642.1:p.Arg3006Gln
XM_017011154.1:c.9017G>A (REV3L)	XP_016866643.1:p.Arg3006Gln
XR_001743550.2:n.9359G>A (REV3L)
XR_001743552.2:n.9281G>A (REV3L)
XR_001743553.2:n.9677G>A (REV3L)
XR_001743555.2:n.9599G>A (REV3L)
XR_001743556.2:n.9406G>A (REV3L)
XR_002956293.1:n.10617G>A (REV3L)
NM_001286431.2:c.8939G>A (REV3L)	NP_001273360.1:p.Arg2980Gln
NM_001372078.1:c.9173G>A (REV3L) MANE Select	NP_001359007.1:p.Arg3058Gln
NM_001286432.2:c.8939G>A (REV3L)	NP_001273361.1:p.Arg2980Gln
NM_002912.5:c.9173G>A (REV3L)	NP_002903.3:p.Arg3058Gln