Canonical Allele Identifier: CA2677949807
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31269543-CCT-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269544_31269545del , CM000668.2:g.31269544_31269545del GRCh38
NC_000006.11:g.31237321_31237322del , CM000668.1:g.31237321_31237322del GRCh37
NC_000006.10:g.31345300_31345301del NCBI36
NG_029422.2:g.7587_7588del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1016-20_1016-19del MANE Select ENSP00000365402.5:n.1016-20_1016-19del
ENST00000376228.9:c.1016-20_1016-19del ENSP00000365402.5:n.1016-20_1016-19del
ENST00000376237.8:c.*603-20_*603-19del ENSP00000365412.4:n.*603-20_*603-19del
ENST00000383329.7:c.1016-2_1016-1del ENSP00000372819.3:n.1016-2_1016-1del
ENST00000466892.5:n.122_123del
ENST00000470363.5:n.754_755del
ENST00000487245.5:n.1375-20_1375-19del
NM_002117.5:c.1016-20_1016-19del NP_002108.4:n.1016-20_1016-19del
NM_002117.6:c.1016-20_1016-19del MANE Select NP_002108.4:n.1016-20_1016-19del
Search 100 bp 5'
Search 100 bp 3'