Canonical Allele Identifier: CA2770491161
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270354_31270355insAGC , CM000668.2:g.31270354_31270355insAGC GRCh38
NC_000006.11:g.31238131_31238132insAGC , CM000668.1:g.31238131_31238132insAGC GRCh37
NC_000006.10:g.31346110_31346111insAGC NCBI36
NG_029422.2:g.6778_6779insCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.751_752insCTG MANE Select ENSP00000365402.5:p.Gln250_Asp251insAla
ENST00000376228.9:c.751_752insCTG ENSP00000365402.5:p.Gln250_Asp251insAla
ENST00000376237.8:c.*338_*339insCTG ENSP00000365412.4:n.*338_*339insCTG
ENST00000383329.7:c.751_752insCTG ENSP00000372819.3:p.Gln250_Asp251insAla
ENST00000415537.1:c.665-23_665-22insCTG
ENST00000470363.5:n.69_70insCTG
ENST00000487245.5:n.1110_1111insCTG
ENST00000495835.1:n.940_941insCTG
NM_002117.5:c.751_752insCTG NP_002108.4:p.Gln250_Asp251insAla
NM_002117.6:c.751_752insCTG MANE Select NP_002108.4:p.Gln250_Asp251insAla