Canonical Allele Identifier: CA2677951695
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31271611-GGTT-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271614_31271616del , CM000668.2:g.31271614_31271616del GRCh38
NC_000006.11:g.31239391_31239393del , CM000668.1:g.31239391_31239393del GRCh37
NC_000006.10:g.31347370_31347372del NCBI36
NG_029422.2:g.5518_5520del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.328_330del MANE Select ENSP00000365402.5:p.Asn110del
ENST00000376228.9:c.328_330del ENSP00000365402.5:p.Asn110del
ENST00000376237.8:c.328_330del ENSP00000365412.4:p.Asn110del
ENST00000383329.7:c.328_330del ENSP00000372819.3:p.Asn110del
ENST00000415537.1:c.326_328del
ENST00000484378.1:n.347_349del
ENST00000487245.5:n.437_439del
ENST00000495835.1:n.517_519del
NM_002117.5:c.328_330del NP_002108.4:p.Asn110del
NM_002117.6:c.328_330del MANE Select NP_002108.4:p.Asn110del
Search 100 bp 5'
Search 100 bp 3'