Canonical Allele Identifier: CA3710637
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs769412202

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271029del , CM000668.2:g.31271029del GRCh38
NC_000006.11:g.31238806del , CM000668.1:g.31238806del GRCh37
NC_000006.10:g.31346785del NCBI36
NG_029422.2:g.6105del

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.619+46del MANE Select ENSP00000365402.5:n.619+46del
ENST00000376228.9:c.619+46del ENSP00000365402.5:n.619+46del
ENST00000376237.8:c.*206+46del ENSP00000365412.4:n.*206+46del
ENST00000383329.7:c.619+46del ENSP00000372819.3:n.619+46del
ENST00000415537.1:c.617+46del
ENST00000487245.5:n.978+46del
ENST00000495835.1:n.808+46del
NM_002117.5:c.619+46del NP_002108.4:n.619+46del
NM_002117.6:c.619+46del MANE Select NP_002108.4:n.619+46del