Canonical Allele Identifier: CA451780765

Gene: REV3L MFSD4B

Linked Data

• COSMIC: COSM5423309 ; COSM5423310
• MyVariant Identifiers: chr6:g.111628750C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111307547C>G , CM000668.2:g.111307547C>G	GRCh38
NC_000006.11:g.111628750C>G , CM000668.1:g.111628750C>G	GRCh37
NC_000006.10:g.111735443C>G	NCBI36
NG_053000.1:g.181169G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368802.8:c.9066G>C (REV3L) MANE Select	ENSP00000357792.3:p.Ser3022=
ENST00000666581.2:n.277+29389C>G (MFSD4B)
ENST00000673245.1:n.273+11772C>G (MFSD4B)
ENST00000673446.1:n.179+39710C>G (MFSD4B)
ENST00000358835.7:c.9066G>C (REV3L)	ENSP00000351697.3:p.Ser3022=
ENST00000368802.7:c.9066G>C (REV3L)	ENSP00000357792.3:p.Ser3022=
ENST00000368805.5:c.9066G>C (REV3L)	ENSP00000357795.1:p.Ser3022=
ENST00000422377.5:c.*9050G>C (REV3L)	ENSP00000393184.1:n.*9050G>C
ENST00000434009.5:c.*9157G>C (REV3L)	ENSP00000391605.1:n.*9157G>C
ENST00000435970.5:c.8832G>C (REV3L)	ENSP00000402003.1:p.Ser2944=
ENST00000462119.5:n.1203G>C (REV3L)
NM_001286431.1:c.8832G>C (REV3L)	NP_001273360.1:p.Ser2944=
NM_001286432.1:c.8832G>C (REV3L)	NP_001273361.1:p.Ser2944=
NM_002912.4:c.9066G>C (REV3L)	NP_002903.3:p.Ser3022=
XM_006715543.2:c.9066G>C (REV3L)	XP_006715606.1:p.Ser3022=
XM_006715544.2:c.8832G>C (REV3L)	XP_006715607.1:p.Ser2944=
XM_011536028.1:c.9147G>C (REV3L)	XP_011534330.1:p.Ser3049=
XM_011536029.1:c.9144G>C (REV3L)	XP_011534331.1:p.Ser3048=
XM_011536030.1:c.9069G>C (REV3L)	XP_011534332.1:p.Ser3023=
XM_011536031.1:c.8913G>C (REV3L)	XP_011534333.1:p.Ser2971=
XM_011536032.1:c.8913G>C (REV3L)	XP_011534334.1:p.Ser2971=
XR_942871.1:n.2045+29389C>G
XM_011536028.2:c.9147G>C (REV3L)	XP_011534330.1:p.Ser3049=
XM_011536029.3:c.9144G>C (REV3L)	XP_011534331.1:p.Ser3048=
XM_011536030.3:c.9069G>C (REV3L)	XP_011534332.1:p.Ser3023=
XM_011536031.3:c.8913G>C (REV3L)	XP_011534333.1:p.Ser2971=
XM_011536032.2:c.8913G>C (REV3L)	XP_011534334.1:p.Ser2971=
XM_017011152.2:c.8910G>C (REV3L)	XP_016866641.1:p.Ser2970=
XM_017011153.1:c.8910G>C (REV3L)	XP_016866642.1:p.Ser2970=
XM_017011154.1:c.8910G>C (REV3L)	XP_016866643.1:p.Ser2970=
XR_001743550.2:n.9252G>C (REV3L)
XR_001743552.2:n.9174G>C (REV3L)
XR_001743553.2:n.9570G>C (REV3L)
XR_001743555.2:n.9492G>C (REV3L)
XR_001743556.2:n.9299G>C (REV3L)
XR_002956293.1:n.10510G>C (REV3L)
NM_001286431.2:c.8832G>C (REV3L)	NP_001273360.1:p.Ser2944=
NM_001372078.1:c.9066G>C (REV3L) MANE Select	NP_001359007.1:p.Ser3022=
NM_001286432.2:c.8832G>C (REV3L)	NP_001273361.1:p.Ser2944=
NM_002912.5:c.9066G>C (REV3L)	NP_002903.3:p.Ser3022=