Canonical Allele Identifier: CA917710716
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs1554182959

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271498_31271500dup , CM000668.2:g.31271498_31271500dup GRCh38
NC_000006.11:g.31239275_31239277dup , CM000668.1:g.31239275_31239277dup GRCh37
NC_000006.10:g.31347254_31347256dup NCBI36
NG_029422.2:g.5634_5636dup

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.343+101_343+103dup MANE Select ENSP00000365402.5:n.343+101_343+103dup
ENST00000376228.9:c.343+101_343+103dup ENSP00000365402.5:n.343+101_343+103dup
ENST00000376237.8:c.343+101_343+103dup ENSP00000365412.4:n.343+101_343+103dup
ENST00000383329.7:c.343+101_343+103dup ENSP00000372819.3:n.343+101_343+103dup
ENST00000415537.1:c.341+101_341+103dup
ENST00000484378.1:n.463_465dup
ENST00000487245.5:n.553_555dup
ENST00000495835.1:n.532+101_532+103dup
NM_002117.5:c.343+101_343+103dup NP_002108.4:n.343+101_343+103dup
NM_002117.6:c.343+101_343+103dup MANE Select NP_002108.4:n.343+101_343+103dup