Canonical Allele Identifier: CA2711332889

Gene: HLA-C

Linked Data

• dbSNP Id: rs2113902650

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269514_31269520del , CM000668.2:g.31269514_31269520del	GRCh38
NC_000006.11:g.31237291_31237297del , CM000668.1:g.31237291_31237297del	GRCh37
NC_000006.10:g.31345270_31345276del	NCBI36
NG_029422.2:g.7612_7618del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.1021_1027del MANE Select	ENSP00000365402.5:p.Lys341GlyfsTer?
ENST00000376228.9:c.1021_1027del	ENSP00000365402.5:p.Lys341GlyfsTer?
ENST00000376237.8:c.*608_*614del	ENSP00000365412.4:n.*608_*614del
ENST00000383329.7:c.1039_1045del	ENSP00000372819.3:p.Lys347GlyfsTer?
ENST00000466892.5:n.147_153del
ENST00000470363.5:n.779_785del
ENST00000487245.5:n.1380_1386del
NM_002117.5:c.1021_1027del	NP_002108.4:p.Lys341GlyfsTer?
NM_002117.6:c.1021_1027del MANE Select	NP_002108.4:p.Lys341GlyfsTer?