Canonical Allele Identifier: CA1619079937
Gene: HLA-C HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270439_31270440delinsCT , CM000668.2:g.31270439_31270440delinsCT GRCh38
NC_000006.11:g.31238216_31238217delinsCT , CM000668.1:g.31238216_31238217delinsCT GRCh37
NC_000006.10:g.31346195_31346196delinsCT NCBI36
NG_029422.2:g.6692_6693delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.665_666delinsAG MANE Select ENSP00000365402.5:p.Glu222=
ENST00000376228.9:c.665_666delinsAG ENSP00000365402.5:p.Glu222=
ENST00000376237.8:c.*252_*253delinsAG ENSP00000365412.4:n.*252_*253delinsAG
ENST00000383329.7:c.665_666delinsAG ENSP00000372819.3:p.Glu222=
ENST00000415537.1:c.663_664delinsAG
ENST00000487245.5:n.1024_1025delinsAG
ENST00000495835.1:n.854_855delinsAG
NM_002117.5:c.665_666delinsAG NP_002108.4:p.Glu222=
NM_002117.6:c.665_666delinsAG MANE Select NP_002108.4:p.Glu222=
Search 100 bp 5'
Search 100 bp 3'