Canonical Allele Identifier: CA1087427770
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v3: 6-31271495-TCCA-T
gnomAD v4: 6-31271495-TCCA-T
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271498_31271500del , CM000668.2:g.31271498_31271500del GRCh38
NC_000006.11:g.31239275_31239277del , CM000668.1:g.31239275_31239277del GRCh37
NC_000006.10:g.31347254_31347256del NCBI36
NG_029422.2:g.5634_5636del

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.343+101_343+103del MANE Select ENSP00000365402.5:n.343+101_343+103del
ENST00000376228.9:c.343+101_343+103del ENSP00000365402.5:n.343+101_343+103del
ENST00000376237.8:c.343+101_343+103del ENSP00000365412.4:n.343+101_343+103del
ENST00000383329.7:c.343+101_343+103del ENSP00000372819.3:n.343+101_343+103del
ENST00000415537.1:c.341+101_341+103del
ENST00000484378.1:n.463_465del
ENST00000487245.5:n.553_555del
ENST00000495835.1:n.532+101_532+103del
NM_002117.5:c.343+101_343+103del NP_002108.4:n.343+101_343+103del
NM_002117.6:c.343+101_343+103del MANE Select NP_002108.4:n.343+101_343+103del
Search 100 bp 5'
Search 100 bp 3'