Canonical Allele Identifier: CA365254562

Gene: REV3L MFSD4B

Linked Data

• COSMIC: COSM1439778 ; COSM1439779
• MyVariant Identifiers: chr6:g.111628749G>C (hg19) ; chr6:g.111307546G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111307546G>C , CM000668.2:g.111307546G>C	GRCh38
NC_000006.11:g.111628749G>C , CM000668.1:g.111628749G>C	GRCh37
NC_000006.10:g.111735442G>C	NCBI36
NG_053000.1:g.181170C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368802.8:c.9067C>G (REV3L) MANE Select	ENSP00000357792.3:p.Arg3023Gly
ENST00000666581.2:n.277+29388G>C (MFSD4B)
ENST00000673245.1:n.273+11771G>C (MFSD4B)
ENST00000673446.1:n.179+39709G>C (MFSD4B)
ENST00000358835.7:c.9067C>G (REV3L)	ENSP00000351697.3:p.Arg3023Gly
ENST00000368802.7:c.9067C>G (REV3L)	ENSP00000357792.3:p.Arg3023Gly
ENST00000368805.5:c.9067C>G (REV3L)	ENSP00000357795.1:p.Arg3023Gly
ENST00000422377.5:c.*9051C>G (REV3L)	ENSP00000393184.1:n.*9051C>G
ENST00000434009.5:c.*9158C>G (REV3L)	ENSP00000391605.1:n.*9158C>G
ENST00000435970.5:c.8833C>G (REV3L)	ENSP00000402003.1:p.Arg2945Gly
ENST00000462119.5:n.1204C>G (REV3L)
NM_001286431.1:c.8833C>G (REV3L)	NP_001273360.1:p.Arg2945Gly
NM_001286432.1:c.8833C>G (REV3L)	NP_001273361.1:p.Arg2945Gly
NM_002912.4:c.9067C>G (REV3L)	NP_002903.3:p.Arg3023Gly
XM_006715543.2:c.9067C>G (REV3L)	XP_006715606.1:p.Arg3023Gly
XM_006715544.2:c.8833C>G (REV3L)	XP_006715607.1:p.Arg2945Gly
XM_011536028.1:c.9148C>G (REV3L)	XP_011534330.1:p.Arg3050Gly
XM_011536029.1:c.9145C>G (REV3L)	XP_011534331.1:p.Arg3049Gly
XM_011536030.1:c.9070C>G (REV3L)	XP_011534332.1:p.Arg3024Gly
XM_011536031.1:c.8914C>G (REV3L)	XP_011534333.1:p.Arg2972Gly
XM_011536032.1:c.8914C>G (REV3L)	XP_011534334.1:p.Arg2972Gly
XR_942871.1:n.2045+29388G>C
XM_011536028.2:c.9148C>G (REV3L)	XP_011534330.1:p.Arg3050Gly
XM_011536029.3:c.9145C>G (REV3L)	XP_011534331.1:p.Arg3049Gly
XM_011536030.3:c.9070C>G (REV3L)	XP_011534332.1:p.Arg3024Gly
XM_011536031.3:c.8914C>G (REV3L)	XP_011534333.1:p.Arg2972Gly
XM_011536032.2:c.8914C>G (REV3L)	XP_011534334.1:p.Arg2972Gly
XM_017011152.2:c.8911C>G (REV3L)	XP_016866641.1:p.Arg2971Gly
XM_017011153.1:c.8911C>G (REV3L)	XP_016866642.1:p.Arg2971Gly
XM_017011154.1:c.8911C>G (REV3L)	XP_016866643.1:p.Arg2971Gly
XR_001743550.2:n.9253C>G (REV3L)
XR_001743552.2:n.9175C>G (REV3L)
XR_001743553.2:n.9571C>G (REV3L)
XR_001743555.2:n.9493C>G (REV3L)
XR_001743556.2:n.9300C>G (REV3L)
XR_002956293.1:n.10511C>G (REV3L)
NM_001286431.2:c.8833C>G (REV3L)	NP_001273360.1:p.Arg2945Gly
NM_001372078.1:c.9067C>G (REV3L) MANE Select	NP_001359007.1:p.Arg3023Gly
NM_001286432.2:c.8833C>G (REV3L)	NP_001273361.1:p.Arg2945Gly
NM_002912.5:c.9067C>G (REV3L)	NP_002903.3:p.Arg3023Gly