Canonical Allele Identifier: CA2677950189
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269872_31269884del , CM000668.2:g.31269872_31269884del GRCh38
NC_000006.11:g.31237649_31237661del , CM000668.1:g.31237649_31237661del GRCh37
NC_000006.10:g.31345628_31345640del NCBI36
NG_029422.2:g.7248_7260del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1015+82_1015+94del MANE Select ENSP00000365402.5:n.1015+82_1015+94del
ENST00000376228.9:c.1015+82_1015+94del ENSP00000365402.5:n.1015+82_1015+94del
ENST00000376237.8:c.*602+82_*602+94del ENSP00000365412.4:n.*602+82_*602+94del
ENST00000383329.7:c.1015+82_1015+94del ENSP00000372819.3:n.1015+82_1015+94del
ENST00000470363.5:n.415_427del
ENST00000487245.5:n.1374+82_1374+94del
NM_002117.5:c.1015+82_1015+94del NP_002108.4:n.1015+82_1015+94del
NM_002117.6:c.1015+82_1015+94del MANE Select NP_002108.4:n.1015+82_1015+94del