Canonical Allele Identifier: CA1619077242
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269048_31269049delinsAT , CM000668.2:g.31269048_31269049delinsAT GRCh38
NC_000006.11:g.31236825_31236826delinsAT , CM000668.1:g.31236825_31236826delinsAT GRCh37
NC_000006.10:g.31344804_31344805delinsAT NCBI36
NG_029422.2:g.8083_8084delinsAT

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.*120_*121delinsAT MANE Select ENSP00000365402.5:n.*120_*121delinsAT
ENST00000376228.9:c.*120_*121delinsAT ENSP00000365402.5:n.*120_*121delinsAT
ENST00000376237.8:c.*808_*809delinsAT ENSP00000365412.4:n.*808_*809delinsAT
ENST00000383329.7:c.*120_*121delinsAT ENSP00000372819.3:n.*120_*121delinsAT
ENST00000466892.5:n.454_455delinsAT
ENST00000470363.5:n.979_980delinsAT
ENST00000487245.5:n.1580_1581delinsAT
NM_002117.5:c.*120_*121delinsAT NP_002108.4:n.*120_*121delinsAT
NM_002117.6:c.*120_*121delinsAT MANE Select NP_002108.4:n.*120_*121delinsAT