Canonical Allele Identifier: CA2844096546
Gene: HLA-C HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271097_31271111del , CM000668.2:g.31271097_31271111del GRCh38
NC_000006.11:g.31238874_31238888del , CM000668.1:g.31238874_31238888del GRCh37
NC_000006.10:g.31346853_31346867del NCBI36
NG_029422.2:g.6022_6036del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.582_596del MANE Select ENSP00000365402.5:p.Tyr195_Gly199del
ENST00000376228.9:c.582_596del ENSP00000365402.5:p.Tyr195_Gly199del
ENST00000376237.8:c.*169_*183del ENSP00000365412.4:n.*169_*183del
ENST00000383329.7:c.582_596del ENSP00000372819.3:p.Tyr195_Gly199del
ENST00000415537.1:c.580_594del
ENST00000487245.5:n.941_955del
ENST00000495835.1:n.771_785del
NM_002117.5:c.582_596del NP_002108.4:p.Tyr195_Gly199del
NM_002117.6:c.582_596del MANE Select NP_002108.4:p.Tyr195_Gly199del
Search 100 bp 5'
Search 100 bp 3'