Canonical Allele Identifier: CA1618466653

Gene: HLA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29830855C= , CM000668.2:g.29830855C=	GRCh38
NC_000006.11:g.29798632C= , CM000668.1:g.29798632C=	GRCh37
NC_000006.10:g.29906611C=	NCBI36
NG_029039.1:g.8877C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360323.11:c.*116C= MANE Select	ENSP00000353472.6:n.*116C=
ENST00000360323.10:c.*116C=	ENSP00000353472.6:n.*116C=
ENST00000376815.3:c.581C=	ENSP00000366011.3:n.581C=
ENST00000376818.7:c.857C=	ENSP00000366014.3:n.857C=
ENST00000376828.6:c.*116C=	ENSP00000366024.2:n.*116C=
ENST00000428701.5:c.*116C=	ENSP00000412927.1:n.*116C=
ENST00000478355.5:n.1255C=
ENST00000478519.5:c.905C=	ENSP00000436375.1:n.905C=
NM_002127.5:c.*116C=	NP_002118.1:n.*116C=
NM_001363567.1:c.*116C=	NP_001350496.1:n.*116C=
XM_017010817.1:c.*116C=	XP_016866306.1:n.*116C=
NM_001363567.2:c.*116C=	NP_001350496.1:n.*116C=
NM_001384280.1:c.*116C=	NP_001371209.1:n.*116C=
NM_001384290.1:c.*116C= MANE Select	NP_001371219.1:n.*116C=
NM_002127.6:c.*116C=	NP_002118.1:n.*116C=