Canonical Allele Identifier: CA136866279
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs796584119

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271037_31271038delinsCG , CM000668.2:g.31271037_31271038delinsCG GRCh38
NC_000006.11:g.31238814_31238815delinsCG , CM000668.1:g.31238814_31238815delinsCG GRCh37
NC_000006.10:g.31346793_31346794delinsCG NCBI36
NG_029422.2:g.6094_6095delinsCG

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.619+35_619+36delinsCG MANE Select ENSP00000365402.5:n.619+35_619+36delinsCG...
ENST00000376228.9:c.619+35_619+36delinsCG ENSP00000365402.5:n.619+35_619+36delinsCG...
ENST00000376237.8:c.*206+35_*206+36delinsCG ENSP00000365412.4:n.*206+35_*206+36delins...
ENST00000383329.7:c.619+35_619+36delinsCG ENSP00000372819.3:n.619+35_619+36delinsCG...
ENST00000415537.1:c.617+35_617+36delinsCG
ENST00000487245.5:n.978+35_978+36delinsCG
ENST00000495835.1:n.808+35_808+36delinsCG
NM_002117.5:c.619+35_619+36delinsCG NP_002108.4:n.619+35_619+36delinsCG
NM_002117.6:c.619+35_619+36delinsCG MANE Select NP_002108.4:n.619+35_619+36delinsCG