Canonical Allele Identifier: CA2711335609
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs2113911891

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271350del , CM000668.2:g.31271350del GRCh38
NC_000006.11:g.31239127del , CM000668.1:g.31239127del GRCh37
NC_000006.10:g.31347106del NCBI36
NG_029422.2:g.5782del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.344-2del MANE Select ENSP00000365402.5:n.344-2del
ENST00000376228.9:c.344-2del ENSP00000365402.5:n.344-2del
ENST00000376237.8:c.344-19del ENSP00000365412.4:n.344-19del
ENST00000383329.7:c.344-2del ENSP00000372819.3:n.344-2del
ENST00000415537.1:c.342-2del
ENST00000484378.1:n.611del
ENST00000487245.5:n.701del
ENST00000495835.1:n.533-2del
NM_002117.5:c.344-2del NP_002108.4:n.344-2del
NM_002117.6:c.344-2del MANE Select NP_002108.4:n.344-2del