Canonical Allele Identifier: CA2677951598
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31271526-CTCT-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271527_31271529del , CM000668.2:g.31271527_31271529del GRCh38
NC_000006.11:g.31239304_31239306del , CM000668.1:g.31239304_31239306del GRCh37
NC_000006.10:g.31347283_31347285del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.343+70_343+72del MANE Select ENSP00000365402.5:n.343+70_343+72del
ENST00000376228.9:c.343+70_343+72del ENSP00000365402.5:n.343+70_343+72del
ENST00000376237.8:c.343+70_343+72del ENSP00000365412.4:n.343+70_343+72del
ENST00000383329.7:c.343+70_343+72del ENSP00000372819.3:n.343+70_343+72del
ENST00000415537.1:c.341+70_341+72del
ENST00000484378.1:n.432_434del
ENST00000487245.5:n.522_524del
ENST00000495835.1:n.532+70_532+72del
NM_002117.5:c.343+70_343+72del NP_002108.4:n.343+70_343+72del
NM_002117.6:c.343+70_343+72del MANE Select NP_002108.4:n.343+70_343+72del
Search 100 bp 5'
Search 100 bp 3'