Canonical Allele Identifier: CA1087426160
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271048_31271049del , CM000668.2:g.31271048_31271049del GRCh38
NC_000006.11:g.31238825_31238826del , CM000668.1:g.31238825_31238826del GRCh37
NC_000006.10:g.31346804_31346805del NCBI36
NG_029422.2:g.6083_6084del

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.619+24_619+25del MANE Select ENSP00000365402.5:n.619+24_619+25del
ENST00000376228.9:c.619+24_619+25del ENSP00000365402.5:n.619+24_619+25del
ENST00000376237.8:c.*206+24_*206+25del ENSP00000365412.4:n.*206+24_*206+25del
ENST00000383329.7:c.619+24_619+25del ENSP00000372819.3:n.619+24_619+25del
ENST00000415537.1:c.617+24_617+25del
ENST00000487245.5:n.978+24_978+25del
ENST00000495835.1:n.808+24_808+25del
NM_002117.5:c.619+24_619+25del NP_002108.4:n.619+24_619+25del
NM_002117.6:c.619+24_619+25del MANE Select NP_002108.4:n.619+24_619+25del