Canonical Allele Identifier: CA2677949799
Gene: HLA-C HGNC NCBI

Linked Data

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

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269528_31269529insAGCTCT , CM000668.2:g.31269528_31269529insAGCTCT GRCh38
NC_000006.11:g.31237305_31237306insAGCTCT , CM000668.1:g.31237305_31237306insAGCTCT GRCh37
NC_000006.10:g.31345284_31345285insAGCTCT NCBI36
NG_029422.2:g.7603_7604insAGAGCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1016-4_1016-3insAGAGCT MANE Select ENSP00000365402.5:n.1016-4_1016-3insAGAGCT
ENST00000376228.9:c.1016-4_1016-3insAGAGCT ENSP00000365402.5:n.1016-4_1016-3insAGAGCT
ENST00000376237.8:c.*603-4_*603-3insAGAGCT ENSP00000365412.4:n.*603-4_*603-3insAGAGCT
ENST00000383329.7:c.1030_1031insAGAGCT ENSP00000372819.3:p.Thr344delinsLysSerSer
ENST00000466892.5:n.138_139insAGAGCT
ENST00000470363.5:n.770_771insAGAGCT
ENST00000487245.5:n.1375-4_1375-3insAGAGCT
NM_002117.5:c.1016-4_1016-3insAGAGCT NP_002108.4:n.1016-4_1016-3insAGAGCT
NM_002117.6:c.1016-4_1016-3insAGAGCT MANE Select NP_002108.4:n.1016-4_1016-3insAGAGCT
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