Canonical Allele Identifier: CA2677949352
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269077_31269078insAC , CM000668.2:g.31269077_31269078insAC GRCh38
NC_000006.11:g.31236854_31236855insAC , CM000668.1:g.31236854_31236855insAC GRCh37
NC_000006.10:g.31344833_31344834insAC NCBI36
NG_029422.2:g.8054_8055insGT

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.*91_*92insGT MANE Select ENSP00000365402.5:n.*91_*92insGT
ENST00000376228.9:c.*91_*92insGT ENSP00000365402.5:n.*91_*92insGT
ENST00000376237.8:c.*779_*780insGT ENSP00000365412.4:n.*779_*780insGT
ENST00000383329.7:c.*91_*92insGT ENSP00000372819.3:n.*91_*92insGT
ENST00000466892.5:n.425_426insGT
ENST00000470363.5:n.950_951insGT
ENST00000487245.5:n.1551_1552insGT
NM_002117.5:c.*91_*92insGT NP_002108.4:n.*91_*92insGT
NM_002117.6:c.*91_*92insGT MANE Select NP_002108.4:n.*91_*92insGT