Canonical Allele Identifier: CA2677950282
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31269987-T-TCAC
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269989_31269990insCCA , CM000668.2:g.31269989_31269990insCCA GRCh38
NC_000006.11:g.31237766_31237767insCCA , CM000668.1:g.31237766_31237767insCCA GRCh37
NC_000006.10:g.31345745_31345746insCCA NCBI36
NG_029422.2:g.7144_7145insGTG

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.993_994insGTG MANE Select ENSP00000365402.5:p.Met331_Met332insVal
ENST00000376228.9:c.993_994insGTG ENSP00000365402.5:p.Met331_Met332insVal
ENST00000376237.8:c.*580_*581insGTG ENSP00000365412.4:n.*580_*581insGTG
ENST00000383329.7:c.993_994insGTG ENSP00000372819.3:p.Met331_Met332insVal
ENST00000470363.5:n.311_312insGTG
ENST00000487245.5:n.1352_1353insGTG
NM_002117.5:c.993_994insGTG NP_002108.4:p.Met331_Met332insVal
NM_002117.6:c.993_994insGTG MANE Select NP_002108.4:p.Met331_Met332insVal
Search 100 bp 5'
Search 100 bp 3'