Canonical Allele Identifier: CA2711332485

Gene: HLA-C

Linked Data

• dbSNP Id: rs2113902282

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269449_31269454del , CM000668.2:g.31269449_31269454del	GRCh38
NC_000006.11:g.31237226_31237231del , CM000668.1:g.31237226_31237231del	GRCh37
NC_000006.10:g.31345205_31345210del	NCBI36
NG_029422.2:g.7678_7683del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.1048+39_1048+44del MANE Select	ENSP00000365402.5:n.1048+39_1048+44del
ENST00000376228.9:c.1048+39_1048+44del	ENSP00000365402.5:n.1048+39_1048+44del
ENST00000376237.8:c.*635+39_*635+44del	ENSP00000365412.4:n.*635+39_*635+44del
ENST00000383329.7:c.1066+39_1066+44del	ENSP00000372819.3:n.1066+39_1066+44del
ENST00000466892.5:n.213_218del
ENST00000470363.5:n.806+39_806+44del
ENST00000487245.5:n.1407+39_1407+44del
NM_002117.5:c.1048+39_1048+44del	NP_002108.4:n.1048+39_1048+44del
NM_002117.6:c.1048+39_1048+44del MANE Select	NP_002108.4:n.1048+39_1048+44del