Canonical Allele Identifier: CA3691917

Gene: HLA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29829503G>A , CM000668.2:g.29829503G>A	GRCh38
NC_000006.11:g.29797280G>A , CM000668.1:g.29797280G>A	GRCh37
NC_000006.10:g.29905259G>A	NCBI36
NG_029039.1:g.7525G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000428701.6:n.809G>A
ENST00000360323.11:c.705G>A MANE Select	ENSP00000353472.6:p.Ala235=
ENST00000360323.10:c.705G>A	ENSP00000353472.6:p.Ala235=
ENST00000376815.3:c.344-313G>A	ENSP00000366011.3:n.344-313G>A
ENST00000376818.7:c.429G>A	ENSP00000366014.3:p.Ala143=
ENST00000376828.6:c.720G>A	ENSP00000366024.2:p.Ala240=
ENST00000428701.5:c.705G>A	ENSP00000412927.1:p.Ala235=
ENST00000478355.5:n.705G>A
ENST00000478519.5:c.429G>A	ENSP00000436375.1:p.Ala143=
NM_002127.5:c.705G>A	NP_002118.1:p.Ala235=
NM_001363567.1:c.720G>A	NP_001350496.1:p.Ala240=
XM_017010817.1:c.429G>A	XP_016866306.1:p.Ala143=
XM_017010818.1:c.429G>A	XP_016866307.1:p.Ala143=
XM_024446420.1:c.705G>A	XP_024302188.1:p.Ala235=
NM_001363567.2:c.720G>A	NP_001350496.1:p.Ala240=
NM_001384280.1:c.720G>A	NP_001371209.1:p.Ala240=
NM_001384290.1:c.705G>A MANE Select	NP_001371219.1:p.Ala235=
NM_002127.6:c.705G>A	NP_002118.1:p.Ala235=