Canonical Allele Identifier: CA3691731

Gene: HLA-G HCG4P8

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29828150G>A , CM000668.2:g.29828150G>A	GRCh38
NC_000006.11:g.29795927G>A , CM000668.1:g.29795927G>A	GRCh37
NC_000006.10:g.29903906G>A	NCBI36
NG_029039.1:g.6172G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001384290.1:c.177G>A (HLA-G) MANE Select	NP_001371219.1:p.Arg59=
ENST00000360323.11:c.177G>A (HLA-G) MANE Select	ENSP00000353472.6:p.Arg59=
NM_001363567.1:c.192G>A (HLA-G)	NP_001350496.1:p.Arg64=
NM_001363567.2:c.192G>A (HLA-G)	NP_001350496.1:p.Arg64=
NM_001384280.1:c.192G>A (HLA-G)	NP_001371209.1:p.Arg64=
NM_002127.5:c.177G>A (HLA-G)	NP_002118.1:p.Arg59=
NM_002127.6:c.177G>A (HLA-G)	NP_002118.1:p.Arg59=
ENST00000360323.10:c.177G>A (HLA-G)	ENSP00000353472.6:p.Arg59=
ENST00000376815.3:c.177G>A (HLA-G)	ENSP00000366011.3:p.Arg59=
ENST00000376818.7:c.177G>A (HLA-G)	ENSP00000366014.3:p.Arg59=
ENST00000376828.6:c.192G>A (HLA-G)	ENSP00000366024.2:p.Arg64=
ENST00000428701.5:c.177G>A (HLA-G)	ENSP00000412927.1:p.Arg59=
ENST00000428701.6:n.355G>A (HLA-G)
ENST00000443049.1:n.215C>T (HCG4P8)
ENST00000478355.5:n.177G>A (HLA-G)
ENST00000478519.5:c.177G>A (HLA-G)	ENSP00000436375.1:p.Arg59=
XM_017010817.1:c.177G>A (HLA-G)	XP_016866306.1:p.Arg59=
XM_017010818.1:c.177G>A (HLA-G)	XP_016866307.1:p.Arg59=
XM_024446420.1:c.177G>A (HLA-G)	XP_024302188.1:p.Arg59=