Canonical Allele Identifier: CA566688982

Gene: HLA-C

Linked Data

• gnomAD v2: 6-31238898-ACTCCACGCACGTGCC-A
• MyVariant Identifiers: chr6:g.31238899_31238913del (hg19) ; chr6:g.31271122_31271136del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271127_31271141del , CM000668.2:g.31271127_31271141del	GRCh38
NC_000006.11:g.31238904_31238918del , CM000668.1:g.31238904_31238918del	GRCh37
NC_000006.10:g.31346883_31346897del	NCBI36
NG_029422.2:g.5996_6010del

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.556_570del MANE Select	ENSP00000365402.5:p.Gly186_Glu190del
ENST00000376228.9:c.556_570del	ENSP00000365402.5:p.Gly186_Glu190del
ENST00000376237.8:c.*143_*157del	ENSP00000365412.4:n.*143_*157del
ENST00000383329.7:c.556_570del	ENSP00000372819.3:p.Gly186_Glu190del
ENST00000415537.1:c.554_568del
ENST00000484378.1:n.825_839del
ENST00000487245.5:n.915_929del
ENST00000495835.1:n.745_759del
NM_002117.5:c.556_570del	NP_002108.4:p.Gly186_Glu190del
NM_002117.6:c.556_570del MANE Select	NP_002108.4:p.Gly186_Glu190del