Canonical Allele Identifier: CA1618466657

Gene: HLA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29830857C= , CM000668.2:g.29830857C=	GRCh38
NC_000006.11:g.29798634C= , CM000668.1:g.29798634C=	GRCh37
NC_000006.10:g.29906613C=	NCBI36
NG_029039.1:g.8879C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001384290.1:c.*118C= MANE Select	NP_001371219.1:n.*118C=
ENST00000360323.11:c.*118C= MANE Select	ENSP00000353472.6:n.*118C=
NM_001363567.1:c.*118C=	NP_001350496.1:n.*118C=
NM_001363567.2:c.*118C=	NP_001350496.1:n.*118C=
NM_001384280.1:c.*118C=	NP_001371209.1:n.*118C=
NM_002127.5:c.*118C=	NP_002118.1:n.*118C=
NM_002127.6:c.*118C=	NP_002118.1:n.*118C=
ENST00000360323.10:c.*118C=	ENSP00000353472.6:n.*118C=
ENST00000376815.3:c.583C=	ENSP00000366011.3:n.583C=
ENST00000376818.7:c.859C=	ENSP00000366014.3:n.859C=
ENST00000376828.6:c.*118C=	ENSP00000366024.2:n.*118C=
ENST00000428701.5:c.*118C=	ENSP00000412927.1:n.*118C=
ENST00000478355.5:n.1257C=
ENST00000478519.5:c.907C=	ENSP00000436375.1:n.907C=
XM_017010817.1:c.*118C=	XP_016866306.1:n.*118C=