Canonical Allele Identifier: CA2677950501
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270121_31270122insA , CM000668.2:g.31270121_31270122insA GRCh38
NC_000006.11:g.31237898_31237899insA , CM000668.1:g.31237898_31237899insA GRCh37
NC_000006.10:g.31345877_31345878insA NCBI36
NG_029422.2:g.7010_7011insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.896-37_896-36insT MANE Select ENSP00000365402.5:n.896-37_896-36insT
ENST00000376228.9:c.896-37_896-36insT ENSP00000365402.5:n.896-37_896-36insT
ENST00000376237.8:c.*483-37_*483-36insT ENSP00000365412.4:n.*483-37_*483-36insT
ENST00000383329.7:c.896-37_896-36insT ENSP00000372819.3:n.896-37_896-36insT
ENST00000470363.5:n.214-37_214-36insT
ENST00000487245.5:n.1255-37_1255-36insT
NM_002117.5:c.896-37_896-36insT NP_002108.4:n.896-37_896-36insT
NM_002117.6:c.896-37_896-36insT MANE Select NP_002108.4:n.896-37_896-36insT