Canonical Allele Identifier: CA2770491572

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271582_31271583insA , CM000668.2:g.31271582_31271583insA	GRCh38
NC_000006.11:g.31239359_31239360insA , CM000668.1:g.31239359_31239360insA	GRCh37
NC_000006.10:g.31347338_31347339insA	NCBI36
NG_029422.2:g.5549_5550insT

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.343+16_343+17insT MANE Select	ENSP00000365402.5:n.343+16_343+17insT
ENST00000376228.9:c.343+16_343+17insT	ENSP00000365402.5:n.343+16_343+17insT
ENST00000376237.8:c.343+16_343+17insT	ENSP00000365412.4:n.343+16_343+17insT
ENST00000383329.7:c.343+16_343+17insT	ENSP00000372819.3:n.343+16_343+17insT
ENST00000415537.1:c.341+16_341+17insT
ENST00000484378.1:n.378_379insT
ENST00000487245.5:n.468_469insT
ENST00000495835.1:n.532+16_532+17insT
NM_002117.5:c.343+16_343+17insT	NP_002108.4:n.343+16_343+17insT
NM_002117.6:c.343+16_343+17insT MANE Select	NP_002108.4:n.343+16_343+17insT