Canonical Allele Identifier: CA2677950292
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31269991-AGCGGTG-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269992_31269997del , CM000668.2:g.31269992_31269997del GRCh38
NC_000006.11:g.31237769_31237774del , CM000668.1:g.31237769_31237774del GRCh37
NC_000006.10:g.31345748_31345753del NCBI36
NG_029422.2:g.7135_7140del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.984_989del MANE Select ENSP00000365402.5:p.Thr329_Ala330del
ENST00000376228.9:c.984_989del ENSP00000365402.5:p.Thr329_Ala330del
ENST00000376237.8:c.*571_*576del ENSP00000365412.4:n.*571_*576del
ENST00000383329.7:c.984_989del ENSP00000372819.3:p.Thr329_Ala330del
ENST00000470363.5:n.302_307del
ENST00000487245.5:n.1343_1348del
NM_002117.5:c.984_989del NP_002108.4:p.Thr329_Ala330del
NM_002117.6:c.984_989del MANE Select NP_002108.4:p.Thr329_Ala330del
Search 100 bp 5'
Search 100 bp 3'