Canonical Allele Identifier: CA1618466502

Gene: HLA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29830642G= , CM000668.2:g.29830642G=	GRCh38
NC_000006.11:g.29798419G= , CM000668.1:g.29798419G=	GRCh37
NC_000006.10:g.29906398G=	NCBI36
NG_029039.1:g.8664G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001384290.1:c.*29-126G= MANE Select	NP_001371219.1:n.*29-126G=
ENST00000360323.11:c.*29-126G= MANE Select	ENSP00000353472.6:n.*29-126G=
NM_001363567.1:c.*29-126G=	NP_001350496.1:n.*29-126G=
NM_001363567.2:c.*29-126G=	NP_001350496.1:n.*29-126G=
NM_001384280.1:c.*29-126G=	NP_001371209.1:n.*29-126G=
NM_002127.5:c.*29-126G=	NP_002118.1:n.*29-126G=
NM_002127.6:c.*29-126G=	NP_002118.1:n.*29-126G=
ENST00000360323.10:c.*29-126G=	ENSP00000353472.6:n.*29-126G=
ENST00000376815.3:c.494-126G=	ENSP00000366011.3:n.494-126G=
ENST00000376818.7:c.770-126G=	ENSP00000366014.3:n.770-126G=
ENST00000376828.6:c.*29-126G=	ENSP00000366024.2:n.*29-126G=
ENST00000428701.5:c.*29-126G=	ENSP00000412927.1:n.*29-126G=
ENST00000478355.5:n.1168-126G=
ENST00000478519.5:c.817+42G=	ENSP00000436375.1:n.817+42G=
XM_017010817.1:c.*29-126G=	XP_016866306.1:n.*29-126G=