Canonical Allele Identifier: CA2677950290
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269990_31269991insCAAC , CM000668.2:g.31269990_31269991insCAAC GRCh38
NC_000006.11:g.31237767_31237768insCAAC , CM000668.1:g.31237767_31237768insCAAC GRCh37
NC_000006.10:g.31345746_31345747insCAAC NCBI36
NG_029422.2:g.7141_7142insGTTG

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.990_991insGTTG MANE Select ENSP00000365402.5:p.Met331ValfsTer5
ENST00000376228.9:c.990_991insGTTG ENSP00000365402.5:p.Met331ValfsTer5
ENST00000376237.8:c.*577_*578insGTTG ENSP00000365412.4:n.*577_*578insGTTG
ENST00000383329.7:c.990_991insGTTG ENSP00000372819.3:p.Met331ValfsTer5
ENST00000470363.5:n.308_309insGTTG
ENST00000487245.5:n.1349_1350insGTTG
NM_002117.5:c.990_991insGTTG NP_002108.4:p.Met331ValfsTer5
NM_002117.6:c.990_991insGTTG MANE Select NP_002108.4:p.Met331ValfsTer5