Canonical Allele Identifier: CA136021399
Gene: HLA-G HGNC NCBI
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Genomic Alleles

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

Transcript Alleles

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