Canonical Allele Identifier: CA2677951255

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31271138-TCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271139_31271140del , CM000668.2:g.31271139_31271140del	GRCh38
NC_000006.11:g.31238916_31238917del , CM000668.1:g.31238916_31238917del	GRCh37
NC_000006.10:g.31346895_31346896del	NCBI36
NG_029422.2:g.5992_5993del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.552_553del MANE Select	ENSP00000365402.5:p.Glu185GlyfsTer?
ENST00000376228.9:c.552_553del	ENSP00000365402.5:p.Glu185GlyfsTer?
ENST00000376237.8:c.*139_*140del	ENSP00000365412.4:n.*139_*140del
ENST00000383329.7:c.552_553del	ENSP00000372819.3:p.Glu185GlyfsTer?
ENST00000415537.1:c.550_551del
ENST00000484378.1:n.821_822del
ENST00000487245.5:n.911_912del
ENST00000495835.1:n.741_742del
NM_002117.5:c.552_553del	NP_002108.4:p.Glu185GlyfsTer?
NM_002117.6:c.552_553del MANE Select	NP_002108.4:p.Glu185GlyfsTer?