Canonical Allele Identifier: CA2677949580
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31269273-TC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269277del , CM000668.2:g.31269277del GRCh38
NC_000006.11:g.31237054del , CM000668.1:g.31237054del GRCh37
NC_000006.10:g.31345033del NCBI36
NG_029422.2:g.7858del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1096+64del MANE Select ENSP00000365402.5:n.1096+64del
ENST00000376228.9:c.1096+64del ENSP00000365402.5:n.1096+64del
ENST00000376237.8:c.*683+64del ENSP00000365412.4:n.*683+64del
ENST00000383329.7:c.1114+64del ENSP00000372819.3:n.1114+64del
ENST00000466892.5:n.329+64del
ENST00000470363.5:n.854+64del
ENST00000487245.5:n.1455+64del
NM_002117.5:c.1096+64del NP_002108.4:n.1096+64del
NM_002117.6:c.1096+64del MANE Select NP_002108.4:n.1096+64del
Search 100 bp 5'
Search 100 bp 3'