Canonical Allele Identifier: CA2677949798
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31269528-G-GAGCTCTTCCTCC
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269528_31269529insAGCTCTTCCTCC , CM000668.2:g.31269528_31269529insAGCTCTTCCTCC GRCh38
NC_000006.11:g.31237305_31237306insAGCTCTTCCTCC , CM000668.1:g.31237305_31237306insAGCTCTTCCTCC GRCh37
NC_000006.10:g.31345284_31345285insAGCTCTTCCTCC NCBI36
NG_029422.2:g.7603_7604insGGAGGAAGAGCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1016-4_1016-3insGGAGGAAGAGCT MANE Select ENSP00000365402.5:n.1016-4_1016-3insGGAGGAAGAGCT
ENST00000376228.9:c.1016-4_1016-3insGGAGGAAGAGCT ENSP00000365402.5:n.1016-4_1016-3insGGAGGAAGAGCT
ENST00000376237.8:c.*603-4_*603-3insGGAGGAAGAGCT ENSP00000365412.4:n.*603-4_*603-3insGGAGGAAGAGCT
ENST00000383329.7:c.1030_1031insGGAGGAAGAGCT ENSP00000372819.3:p.Thr344delinsArgArgLysSerSer
ENST00000466892.5:n.138_139insGGAGGAAGAGCT
ENST00000470363.5:n.770_771insGGAGGAAGAGCT
ENST00000487245.5:n.1375-4_1375-3insGGAGGAAGAGCT
NM_002117.5:c.1016-4_1016-3insGGAGGAAGAGCT NP_002108.4:n.1016-4_1016-3insGGAGGAAGAGCT
NM_002117.6:c.1016-4_1016-3insGGAGGAAGAGCT MANE Select NP_002108.4:n.1016-4_1016-3insGGAGGAAGAGCT
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