Canonical Allele Identifier: CA1087451831
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v3: 6-31269795-TTG-T
gnomAD v4: 6-31269795-TTG-T
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269797_31269798del , CM000668.2:g.31269797_31269798del GRCh38
NC_000006.11:g.31237574_31237575del , CM000668.1:g.31237574_31237575del GRCh37
NC_000006.10:g.31345553_31345554del NCBI36
NG_029422.2:g.7335_7336del

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.1015+169_1015+170del MANE Select ENSP00000365402.5:n.1015+169_1015+170del
ENST00000376228.9:c.1015+169_1015+170del ENSP00000365402.5:n.1015+169_1015+170del
ENST00000376237.8:c.*602+169_*602+170del ENSP00000365412.4:n.*602+169_*602+170del
ENST00000383329.7:c.1015+169_1015+170del ENSP00000372819.3:n.1015+169_1015+170del
ENST00000470363.5:n.502_503del
ENST00000487245.5:n.1374+169_1374+170del
NM_002117.5:c.1015+169_1015+170del NP_002108.4:n.1015+169_1015+170del
NM_002117.6:c.1015+169_1015+170del MANE Select NP_002108.4:n.1015+169_1015+170del
Search 100 bp 5'
Search 100 bp 3'