Canonical Allele Identifier: CA3710402
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs765198307

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270121_31270127del , CM000668.2:g.31270121_31270127del GRCh38
NC_000006.11:g.31237898_31237904del , CM000668.1:g.31237898_31237904del GRCh37
NC_000006.10:g.31345877_31345883del NCBI36
NG_029422.2:g.7007_7013del

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.896-40_896-34del MANE Select ENSP00000365402.5:n.896-40_896-34del
ENST00000376228.9:c.896-40_896-34del ENSP00000365402.5:n.896-40_896-34del
ENST00000376237.8:c.*483-40_*483-34del ENSP00000365412.4:n.*483-40_*483-34del
ENST00000383329.7:c.896-40_896-34del ENSP00000372819.3:n.896-40_896-34del
ENST00000470363.5:n.214-40_214-34del
ENST00000487245.5:n.1255-40_1255-34del
NM_002117.5:c.896-40_896-34del NP_002108.4:n.896-40_896-34del
NM_002117.6:c.896-40_896-34del MANE Select NP_002108.4:n.896-40_896-34del