Canonical Allele Identifier: CA650811083
Gene: HLA-G HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29830840_29830841insC , CM000668.2:g.29830840_29830841insC GRCh38
NC_000006.11:g.29798617_29798618insC , CM000668.1:g.29798617_29798618insC GRCh37
NC_000006.10:g.29906596_29906597insC NCBI36
NG_029039.1:g.8862_8863insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000360323.11:c.*101_*102insC MANE Select ENSP00000353472.6:n.*101_*102insC
ENST00000360323.10:c.*101_*102insC ENSP00000353472.6:n.*101_*102insC
ENST00000376815.3:c.566_567insC ENSP00000366011.3:n.566_567insC
ENST00000376818.7:c.842_843insC ENSP00000366014.3:n.842_843insC
ENST00000376828.6:c.*101_*102insC ENSP00000366024.2:n.*101_*102insC
ENST00000428701.5:c.*101_*102insC ENSP00000412927.1:n.*101_*102insC
ENST00000478355.5:n.1240_1241insC
ENST00000478519.5:c.890_891insC ENSP00000436375.1:n.890_891insC
NM_002127.5:c.*101_*102insC NP_002118.1:n.*101_*102insC
NM_001363567.1:c.*101_*102insC NP_001350496.1:n.*101_*102insC
XM_017010817.1:c.*101_*102insC XP_016866306.1:n.*101_*102insC
NM_001363567.2:c.*101_*102insC NP_001350496.1:n.*101_*102insC
NM_001384280.1:c.*101_*102insC NP_001371209.1:n.*101_*102insC
NM_001384290.1:c.*101_*102insC MANE Select NP_001371219.1:n.*101_*102insC
NM_002127.6:c.*101_*102insC NP_002118.1:n.*101_*102insC