Canonical Allele Identifier: CA365254425

Gene: REV3L MFSD4B

Linked Data

• MyVariant Identifiers: chr6:g.111628685A>G (hg19) ; chr6:g.111307482A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111307482A>G , CM000668.2:g.111307482A>G	GRCh38
NC_000006.11:g.111628685A>G , CM000668.1:g.111628685A>G	GRCh37
NC_000006.10:g.111735378A>G	NCBI36
NG_053000.1:g.181234T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368802.8:c.9131T>C (REV3L) MANE Select	ENSP00000357792.3:p.Val3044Ala
ENST00000666581.2:n.277+29324A>G (MFSD4B)
ENST00000673245.1:n.273+11707A>G (MFSD4B)
ENST00000673446.1:n.179+39645A>G (MFSD4B)
ENST00000358835.7:c.9131T>C (REV3L)	ENSP00000351697.3:p.Val3044Ala
ENST00000368802.7:c.9131T>C (REV3L)	ENSP00000357792.3:p.Val3044Ala
ENST00000368805.5:c.9131T>C (REV3L)	ENSP00000357795.1:p.Val3044Ala
ENST00000422377.5:c.*9115T>C (REV3L)	ENSP00000393184.1:n.*9115T>C
ENST00000434009.5:c.*9222T>C (REV3L)	ENSP00000391605.1:n.*9222T>C
ENST00000435970.5:c.8897T>C (REV3L)	ENSP00000402003.1:p.Val2966Ala
ENST00000462119.5:n.1268T>C (REV3L)
NM_001286431.1:c.8897T>C (REV3L)	NP_001273360.1:p.Val2966Ala
NM_001286432.1:c.8897T>C (REV3L)	NP_001273361.1:p.Val2966Ala
NM_002912.4:c.9131T>C (REV3L)	NP_002903.3:p.Val3044Ala
XM_006715543.2:c.9131T>C (REV3L)	XP_006715606.1:p.Val3044Ala
XM_006715544.2:c.8897T>C (REV3L)	XP_006715607.1:p.Val2966Ala
XM_011536028.1:c.9212T>C (REV3L)	XP_011534330.1:p.Val3071Ala
XM_011536029.1:c.9209T>C (REV3L)	XP_011534331.1:p.Val3070Ala
XM_011536030.1:c.9134T>C (REV3L)	XP_011534332.1:p.Val3045Ala
XM_011536031.1:c.8978T>C (REV3L)	XP_011534333.1:p.Val2993Ala
XM_011536032.1:c.8978T>C (REV3L)	XP_011534334.1:p.Val2993Ala
XR_942871.1:n.2045+29324A>G
XM_011536028.2:c.9212T>C (REV3L)	XP_011534330.1:p.Val3071Ala
XM_011536029.3:c.9209T>C (REV3L)	XP_011534331.1:p.Val3070Ala
XM_011536030.3:c.9134T>C (REV3L)	XP_011534332.1:p.Val3045Ala
XM_011536031.3:c.8978T>C (REV3L)	XP_011534333.1:p.Val2993Ala
XM_011536032.2:c.8978T>C (REV3L)	XP_011534334.1:p.Val2993Ala
XM_017011152.2:c.8975T>C (REV3L)	XP_016866641.1:p.Val2992Ala
XM_017011153.1:c.8975T>C (REV3L)	XP_016866642.1:p.Val2992Ala
XM_017011154.1:c.8975T>C (REV3L)	XP_016866643.1:p.Val2992Ala
XR_001743550.2:n.9317T>C (REV3L)
XR_001743552.2:n.9239T>C (REV3L)
XR_001743553.2:n.9635T>C (REV3L)
XR_001743555.2:n.9557T>C (REV3L)
XR_001743556.2:n.9364T>C (REV3L)
XR_002956293.1:n.10575T>C (REV3L)
NM_001286431.2:c.8897T>C (REV3L)	NP_001273360.1:p.Val2966Ala
NM_001372078.1:c.9131T>C (REV3L) MANE Select	NP_001359007.1:p.Val3044Ala
NM_001286432.2:c.8897T>C (REV3L)	NP_001273361.1:p.Val2966Ala
NM_002912.5:c.9131T>C (REV3L)	NP_002903.3:p.Val3044Ala