Canonical Allele Identifier: CA2677951238

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31271120-CACT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271121_31271123del , CM000668.2:g.31271121_31271123del	GRCh38
NC_000006.11:g.31238898_31238900del , CM000668.1:g.31238898_31238900del	GRCh37
NC_000006.10:g.31346877_31346879del	NCBI36
NG_029422.2:g.6009_6011del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.569_571del MANE Select	ENSP00000365402.5:p.Glu190_Trp191delinsGly
ENST00000376228.9:c.569_571del	ENSP00000365402.5:p.Glu190_Trp191delinsGly
ENST00000376237.8:c.*156_*158del	ENSP00000365412.4:n.*156_*158del
ENST00000383329.7:c.569_571del	ENSP00000372819.3:p.Glu190_Trp191delinsGly
ENST00000415537.1:c.567_569del
ENST00000484378.1:n.838_840del
ENST00000487245.5:n.928_930del
ENST00000495835.1:n.758_760del
NM_002117.5:c.569_571del	NP_002108.4:p.Glu190_Trp191delinsGly
NM_002117.6:c.569_571del MANE Select	NP_002108.4:p.Glu190_Trp191delinsGly