Canonical Allele Identifier: CA2677951178
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271050del , CM000668.2:g.31271050del GRCh38
NC_000006.11:g.31238827del , CM000668.1:g.31238827del GRCh37
NC_000006.10:g.31346806del NCBI36
NG_029422.2:g.6083del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.619+24del MANE Select ENSP00000365402.5:n.619+24del
ENST00000376228.9:c.619+24del ENSP00000365402.5:n.619+24del
ENST00000376237.8:c.*206+24del ENSP00000365412.4:n.*206+24del
ENST00000383329.7:c.619+24del ENSP00000372819.3:n.619+24del
ENST00000415537.1:c.617+24del
ENST00000487245.5:n.978+24del
ENST00000495835.1:n.808+24del
NM_002117.5:c.619+24del NP_002108.4:n.619+24del
NM_002117.6:c.619+24del MANE Select NP_002108.4:n.619+24del