Canonical Allele Identifier: CA365359643

Gene: REV3L MFSD4B

Linked Data

• gnomAD v4: 6-111405488-G-A
• COSMIC: COSM5785414 ; COSM5785415
• MyVariant Identifiers: chr6:g.111726691G>A (hg19) ; chr6:g.111405488G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111405488G>A , CM000668.2:g.111405488G>A	GRCh38
NC_000006.11:g.111726691G>A , CM000668.1:g.111726691G>A	GRCh37
NC_000006.10:g.111833384G>A	NCBI36
NG_053000.1:g.83228C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000368802.8:c.547C>T (REV3L) MANE Select	ENSP00000357792.3:p.Arg183Ter
ENST00000673446.1:n.248-35215G>A (MFSD4B)
ENST00000358835.7:c.547C>T (REV3L)	ENSP00000351697.3:p.Arg183Ter
ENST00000368802.7:c.547C>T (REV3L)	ENSP00000357792.3:p.Arg183Ter
ENST00000368805.5:c.547C>T (REV3L)	ENSP00000357795.1:p.Arg183Ter
ENST00000422377.5:c.*531C>T (REV3L)	ENSP00000393184.1:n.*531C>T
ENST00000434009.5:c.*638C>T (REV3L)	ENSP00000391605.1:n.*638C>T
ENST00000435970.5:c.313C>T (REV3L)	ENSP00000402003.1:p.Arg105Ter
ENST00000460981.1:n.145C>T (REV3L)
ENST00000494858.1:n.220C>T (REV3L)
NM_001286431.1:c.313C>T (REV3L)	NP_001273360.1:p.Arg105Ter
NM_001286432.1:c.313C>T (REV3L)	NP_001273361.1:p.Arg105Ter
NM_002912.4:c.547C>T (REV3L)	NP_002903.3:p.Arg183Ter
XM_006715543.2:c.547C>T (REV3L)	XP_006715606.1:p.Arg183Ter
XM_006715544.2:c.313C>T (REV3L)	XP_006715607.1:p.Arg105Ter
XM_011536028.1:c.547C>T (REV3L)	XP_011534330.1:p.Arg183Ter
XM_011536029.1:c.547C>T (REV3L)	XP_011534331.1:p.Arg183Ter
XM_011536030.1:c.547C>T (REV3L)	XP_011534332.1:p.Arg183Ter
XM_011536031.1:c.313C>T (REV3L)	XP_011534333.1:p.Arg105Ter
XM_011536032.1:c.313C>T (REV3L)	XP_011534334.1:p.Arg105Ter
XM_011536033.1:c.547C>T (REV3L)	XP_011534335.1:p.Arg183Ter
XM_011536034.1:c.547C>T (REV3L)	XP_011534336.1:p.Arg183Ter
XM_011536035.1:c.547C>T (REV3L)	XP_011534337.1:p.Arg183Ter
XM_011536036.1:c.547C>T (REV3L)	XP_011534338.1:p.Arg183Ter
XR_942545.1:n.1096C>T (REV3L)
XR_942546.1:n.1096C>T (REV3L)
XM_011536028.2:c.547C>T (REV3L)	XP_011534330.1:p.Arg183Ter
XM_011536029.3:c.547C>T (REV3L)	XP_011534331.1:p.Arg183Ter
XM_011536030.3:c.547C>T (REV3L)	XP_011534332.1:p.Arg183Ter
XM_011536031.3:c.313C>T (REV3L)	XP_011534333.1:p.Arg105Ter
XM_011536032.2:c.313C>T (REV3L)	XP_011534334.1:p.Arg105Ter
XM_011536036.3:c.547C>T (REV3L)	XP_011534338.1:p.Arg183Ter
XM_017011152.2:c.313C>T (REV3L)	XP_016866641.1:p.Arg105Ter
XM_017011153.1:c.313C>T (REV3L)	XP_016866642.1:p.Arg105Ter
XM_017011154.1:c.313C>T (REV3L)	XP_016866643.1:p.Arg105Ter
XM_017011155.2:c.547C>T (REV3L)	XP_016866644.1:p.Arg183Ter
XR_001743550.2:n.843C>T (REV3L)
XR_001743552.2:n.843C>T (REV3L)
XR_001743553.2:n.843C>T (REV3L)
XR_001743554.2:n.843C>T (REV3L)
XR_001743555.2:n.843C>T (REV3L)
XR_001743556.2:n.843C>T (REV3L)
XR_002956293.1:n.843C>T (REV3L)
NM_001286431.2:c.313C>T (REV3L)	NP_001273360.1:p.Arg105Ter
NM_001372078.1:c.547C>T (REV3L) MANE Select	NP_001359007.1:p.Arg183Ter
NM_001286432.2:c.313C>T (REV3L)	NP_001273361.1:p.Arg105Ter
NM_002912.5:c.547C>T (REV3L)	NP_002903.3:p.Arg183Ter