Canonical Allele Identifier: CA2580592029

Gene: HLA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29830972C>A , CM000668.2:g.29830972C>A	GRCh38
NC_000006.11:g.29798749C>A , CM000668.1:g.29798749C>A	GRCh37
NC_000006.10:g.29906728C>A	NCBI36
NG_029039.1:g.8994C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360323.11:c.*233C>A MANE Select	ENSP00000353472.6:n.*233C>A
ENST00000360323.10:c.*233C>A	ENSP00000353472.6:n.*233C>A
ENST00000376815.3:c.698C>A	ENSP00000366011.3:n.698C>A
ENST00000376818.7:c.974C>A	ENSP00000366014.3:n.974C>A
ENST00000376828.6:c.*233C>A	ENSP00000366024.2:n.*233C>A
ENST00000428701.5:c.*233C>A	ENSP00000412927.1:n.*233C>A
ENST00000478355.5:n.1372C>A
ENST00000478519.5:c.1022C>A	ENSP00000436375.1:n.1022C>A
NM_002127.5:c.*233C>A	NP_002118.1:n.*233C>A
NM_001363567.1:c.*233C>A	NP_001350496.1:n.*233C>A
XM_017010817.1:c.*233C>A	XP_016866306.1:n.*233C>A
NM_001363567.2:c.*233C>A	NP_001350496.1:n.*233C>A
NM_001384280.1:c.*233C>A	NP_001371209.1:n.*233C>A
NM_001384290.1:c.*233C>A MANE Select	NP_001371219.1:n.*233C>A
NM_002127.6:c.*233C>A	NP_002118.1:n.*233C>A