Canonical Allele Identifier: CA2578557032

Gene: HLA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29828502C>G , CM000668.2:g.29828502C>G	GRCh38
NC_000006.11:g.29796279C>G , CM000668.1:g.29796279C>G	GRCh37
NC_000006.10:g.29904258C>G	NCBI36
NG_029039.1:g.6524C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000428701.6:n.522-115C>G
ENST00000360323.11:c.344-41C>G MANE Select	ENSP00000353472.6:n.344-41C>G
ENST00000360323.10:c.344-41C>G	ENSP00000353472.6:n.344-41C>G
ENST00000376815.3:c.343+186C>G	ENSP00000366011.3:n.343+186C>G
ENST00000376818.7:c.343+186C>G	ENSP00000366014.3:n.343+186C>G
ENST00000376828.6:c.359-41C>G	ENSP00000366024.2:n.359-41C>G
ENST00000428701.5:c.344-41C>G	ENSP00000412927.1:n.344-41C>G
ENST00000478355.5:n.344-41C>G
ENST00000478519.5:c.343+186C>G	ENSP00000436375.1:n.343+186C>G
NM_002127.5:c.344-41C>G	NP_002118.1:n.344-41C>G
NM_001363567.1:c.359-41C>G	NP_001350496.1:n.359-41C>G
XM_017010817.1:c.343+186C>G	XP_016866306.1:n.343+186C>G
XM_017010818.1:c.343+186C>G	XP_016866307.1:n.343+186C>G
XM_024446420.1:c.344-41C>G	XP_024302188.1:n.344-41C>G
NM_001363567.2:c.359-41C>G	NP_001350496.1:n.359-41C>G
NM_001384280.1:c.359-41C>G	NP_001371209.1:n.359-41C>G
NM_001384290.1:c.344-41C>G MANE Select	NP_001371219.1:n.344-41C>G
NM_002127.6:c.344-41C>G	NP_002118.1:n.344-41C>G