Canonical Allele Identifier: CA1619080791
Gene: HLA-C HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271673_31271675delinsTTC , CM000668.2:g.31271673_31271675delinsTTC GRCh38
NC_000006.11:g.31239450_31239452delinsTTC , CM000668.1:g.31239450_31239452delinsTTC GRCh37
NC_000006.10:g.31347429_31347431delinsTTC NCBI36
NG_029422.2:g.5457_5459delinsGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.267_269delinsGAA MANE Select ENSP00000365402.5:p.Gln89=
ENST00000376228.9:c.267_269delinsGAA ENSP00000365402.5:p.Gln89=
ENST00000376237.8:c.267_269delinsGAA ENSP00000365412.4:p.Gln89=
ENST00000383329.7:c.267_269delinsGAA ENSP00000372819.3:p.Gln89=
ENST00000415537.1:c.265_267delinsGAA
ENST00000484378.1:n.286_288delinsGAA
ENST00000487245.5:n.376_378delinsGAA
ENST00000495835.1:n.456_458delinsGAA
NM_002117.5:c.267_269delinsGAA NP_002108.4:p.Gln89=
NM_002117.6:c.267_269delinsGAA MANE Select NP_002108.4:p.Gln89=
Search 100 bp 5'
Search 100 bp 3'