Canonical Allele Identifier: CA1618464519

Gene: HLA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29828698T= , CM000668.2:g.29828698T=	GRCh38
NC_000006.11:g.29796475T= , CM000668.1:g.29796475T=	GRCh37
NC_000006.10:g.29904454T=	NCBI36
NG_029039.1:g.6720T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000428701.6:n.603T=
ENST00000360323.11:c.499T= MANE Select	ENSP00000353472.6:p.Ser167=
ENST00000360323.10:c.499T=	ENSP00000353472.6:p.Ser167=
ENST00000376815.3:c.343+382T=	ENSP00000366011.3:n.343+382T=
ENST00000376818.7:c.343+382T=	ENSP00000366014.3:n.343+382T=
ENST00000376828.6:c.514T=	ENSP00000366024.2:p.Ser172=
ENST00000428701.5:c.499T=	ENSP00000412927.1:p.Ser167=
ENST00000478355.5:n.499T=
ENST00000478519.5:c.343+382T=	ENSP00000436375.1:n.343+382T=
NM_002127.5:c.499T=	NP_002118.1:p.Ser167=
NM_001363567.1:c.514T=	NP_001350496.1:p.Ser172=
XM_017010817.1:c.343+382T=	XP_016866306.1:n.343+382T=
XM_017010818.1:c.343+382T=	XP_016866307.1:n.343+382T=
XM_024446420.1:c.499T=	XP_024302188.1:p.Ser167=
NM_001363567.2:c.514T=	NP_001350496.1:p.Ser172=
NM_001384280.1:c.514T=	NP_001371209.1:p.Ser172=
NM_001384290.1:c.499T= MANE Select	NP_001371219.1:p.Ser167=
NM_002127.6:c.499T=	NP_002118.1:p.Ser167=