Canonical Allele Identifier: CA2677781551

Gene: HLA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29830804_29830805insAT , CM000668.2:g.29830804_29830805insAT	GRCh38
NC_000006.11:g.29798581_29798582insAT , CM000668.1:g.29798581_29798582insAT	GRCh37
NC_000006.10:g.29906560_29906561insAT	NCBI36
NG_029039.1:g.8826_8827insAT

Transcript Alleles

HGVS	Amino-acid Change
NM_001384290.1:c.*65_*66insAT MANE Select	NP_001371219.1:n.*65_*66insAT
ENST00000360323.11:c.*65_*66insAT MANE Select	ENSP00000353472.6:n.*65_*66insAT
NM_001363567.1:c.*65_*66insAT	NP_001350496.1:n.*65_*66insAT
NM_001363567.2:c.*65_*66insAT	NP_001350496.1:n.*65_*66insAT
NM_001384280.1:c.*65_*66insAT	NP_001371209.1:n.*65_*66insAT
NM_002127.5:c.*65_*66insAT	NP_002118.1:n.*65_*66insAT
NM_002127.6:c.*65_*66insAT	NP_002118.1:n.*65_*66insAT
ENST00000360323.10:c.*65_*66insAT	ENSP00000353472.6:n.*65_*66insAT
ENST00000376815.3:c.530_531insAT	ENSP00000366011.3:n.530_531insAT
ENST00000376818.7:c.806_807insAT	ENSP00000366014.3:n.806_807insAT
ENST00000376828.6:c.*65_*66insAT	ENSP00000366024.2:n.*65_*66insAT
ENST00000428701.5:c.*65_*66insAT	ENSP00000412927.1:n.*65_*66insAT
ENST00000478355.5:n.1204_1205insAT
ENST00000478519.5:c.854_855insAT	ENSP00000436375.1:n.854_855insAT
XM_017010817.1:c.*65_*66insAT	XP_016866306.1:n.*65_*66insAT