Canonical Allele Identifier: CA2580592024

Gene: HLA-G

Linked Data

• gnomAD v4: 6-29830840-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29830840G>A , CM000668.2:g.29830840G>A	GRCh38
NC_000006.11:g.29798617G>A , CM000668.1:g.29798617G>A	GRCh37
NC_000006.10:g.29906596G>A	NCBI36
NG_029039.1:g.8862G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360323.11:c.*101G>A MANE Select	ENSP00000353472.6:n.*101G>A
ENST00000360323.10:c.*101G>A	ENSP00000353472.6:n.*101G>A
ENST00000376815.3:c.566G>A	ENSP00000366011.3:n.566G>A
ENST00000376818.7:c.842G>A	ENSP00000366014.3:n.842G>A
ENST00000376828.6:c.*101G>A	ENSP00000366024.2:n.*101G>A
ENST00000428701.5:c.*101G>A	ENSP00000412927.1:n.*101G>A
ENST00000478355.5:n.1240G>A
ENST00000478519.5:c.890G>A	ENSP00000436375.1:n.890G>A
NM_002127.5:c.*101G>A	NP_002118.1:n.*101G>A
NM_001363567.1:c.*101G>A	NP_001350496.1:n.*101G>A
XM_017010817.1:c.*101G>A	XP_016866306.1:n.*101G>A
NM_001363567.2:c.*101G>A	NP_001350496.1:n.*101G>A
NM_001384280.1:c.*101G>A	NP_001371209.1:n.*101G>A
NM_001384290.1:c.*101G>A MANE Select	NP_001371219.1:n.*101G>A
NM_002127.6:c.*101G>A	NP_002118.1:n.*101G>A