Canonical Allele Identifier: CA2677950447
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270107_31270108insT , CM000668.2:g.31270107_31270108insT GRCh38
NC_000006.11:g.31237884_31237885insT , CM000668.1:g.31237884_31237885insT GRCh37
NC_000006.10:g.31345863_31345864insT NCBI36
NG_029422.2:g.7024_7025insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.896-23_896-22insA MANE Select ENSP00000365402.5:n.896-23_896-22insA
ENST00000376228.9:c.896-23_896-22insA ENSP00000365402.5:n.896-23_896-22insA
ENST00000376237.8:c.*483-23_*483-22insA ENSP00000365412.4:n.*483-23_*483-22insA
ENST00000383329.7:c.896-23_896-22insA ENSP00000372819.3:n.896-23_896-22insA
ENST00000470363.5:n.214-23_214-22insA
ENST00000487245.5:n.1255-23_1255-22insA
NM_002117.5:c.896-23_896-22insA NP_002108.4:n.896-23_896-22insA
NM_002117.6:c.896-23_896-22insA MANE Select NP_002108.4:n.896-23_896-22insA