Canonical Allele Identifier: CA1619080339

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271130_31271136delinsACGTGCC , CM000668.2:g.31271130_31271136delinsACGTGCC	GRCh38
NC_000006.11:g.31238907_31238913delinsACGTGCC , CM000668.1:g.31238907_31238913delinsACGTGCC	GRCh37
NC_000006.10:g.31346886_31346892delinsACGTGCC	NCBI36
NG_029422.2:g.5996_6002delinsGGCACGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.556_562delinsGGCACGT MANE Select	ENSP00000365402.5:p.Gly186=
ENST00000376228.9:c.556_562delinsGGCACGT	ENSP00000365402.5:p.Gly186=
ENST00000376237.8:c.*143_*149delinsGGCACGT	ENSP00000365412.4:n.*143_*149delinsGGCACGT
ENST00000383329.7:c.556_562delinsGGCACGT	ENSP00000372819.3:p.Gly186=
ENST00000415537.1:c.554_560delinsGGCACGT
ENST00000484378.1:n.825_831delinsGGCACGT
ENST00000487245.5:n.915_921delinsGGCACGT
ENST00000495835.1:n.745_751delinsGGCACGT
NM_002117.5:c.556_562delinsGGCACGT	NP_002108.4:p.Gly186=
NM_002117.6:c.556_562delinsGGCACGT MANE Select	NP_002108.4:p.Gly186=