Canonical Allele Identifier: CA136866482

Gene: HLA-C

Linked Data

• dbSNP Id: rs281860524

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271128_31271136del , CM000668.2:g.31271128_31271136del	GRCh38
NC_000006.11:g.31238905_31238913del , CM000668.1:g.31238905_31238913del	GRCh37
NC_000006.10:g.31346884_31346892del	NCBI36
NG_029422.2:g.5997_6005del

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.557_565del MANE Select	ENSP00000365402.5:p.Gly186_Cys188del
ENST00000376228.9:c.557_565del	ENSP00000365402.5:p.Gly186_Cys188del
ENST00000376237.8:c.*144_*152del	ENSP00000365412.4:n.*144_*152del
ENST00000383329.7:c.557_565del	ENSP00000372819.3:p.Gly186_Cys188del
ENST00000415537.1:c.555_563del
ENST00000484378.1:n.826_834del
ENST00000487245.5:n.916_924del
ENST00000495835.1:n.746_754del
NM_002117.5:c.557_565del	NP_002108.4:p.Gly186_Cys188del
NM_002117.6:c.557_565del MANE Select	NP_002108.4:p.Gly186_Cys188del