Canonical Allele Identifier: CA2677950291
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31269990-TAG-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269991_31269992del , CM000668.2:g.31269991_31269992del GRCh38
NC_000006.11:g.31237768_31237769del , CM000668.1:g.31237768_31237769del GRCh37
NC_000006.10:g.31345747_31345748del NCBI36
NG_029422.2:g.7140_7141del

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.989_990del MANE Select ENSP00000365402.5:p.Ala330AspfsTer4
ENST00000376228.9:c.989_990del ENSP00000365402.5:p.Ala330AspfsTer4
ENST00000376237.8:c.*576_*577del ENSP00000365412.4:n.*576_*577del
ENST00000383329.7:c.989_990del ENSP00000372819.3:p.Ala330AspfsTer4
ENST00000470363.5:n.307_308del
ENST00000487245.5:n.1348_1349del
NM_002117.5:c.989_990del NP_002108.4:p.Ala330AspfsTer4
NM_002117.6:c.989_990del MANE Select NP_002108.4:p.Ala330AspfsTer4
Search 100 bp 5'
Search 100 bp 3'