Canonical Allele Identifier: CA2677949836
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31269576-T-TCTTAGAGCCATGC
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269576_31269577insCTTAGAGCCATGC , CM000668.2:g.31269576_31269577insCTTAGAGCCATGC GRCh38
NC_000006.11:g.31237353_31237354insCTTAGAGCCATGC , CM000668.1:g.31237353_31237354insCTTAGAGCCATGC GRCh37
NC_000006.10:g.31345332_31345333insCTTAGAGCCATGC NCBI36
NG_029422.2:g.7555_7556insGCATGGCTCTAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1016-52_1016-51insGCATGGCTCTAAG MANE Select ENSP00000365402.5:n.1016-52_1016-51insGCATGGCTCTAAG
ENST00000376228.9:c.1016-52_1016-51insGCATGGCTCTAAG ENSP00000365402.5:n.1016-52_1016-51insGCATGGCTCTAAG
ENST00000376237.8:c.*603-52_*603-51insGCATGGCTCTAAG ENSP00000365412.4:n.*603-52_*603-51insGCATGGCTCTAAG
ENST00000383329.7:c.1016-34_1016-33insGCATGGCTCTAAG ENSP00000372819.3:n.1016-34_1016-33insGCATGGCTCTAAG
ENST00000466892.5:n.90_91insGCATGGCTCTAAG
ENST00000470363.5:n.722_723insGCATGGCTCTAAG
ENST00000487245.5:n.1375-52_1375-51insGCATGGCTCTAAG
NM_002117.5:c.1016-52_1016-51insGCATGGCTCTAAG NP_002108.4:n.1016-52_1016-51insGCATGGCTCTAAG
NM_002117.6:c.1016-52_1016-51insGCATGGCTCTAAG MANE Select NP_002108.4:n.1016-52_1016-51insGCATGGCTCTAAG
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