Canonical Allele Identifier: CA2677950617
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270184_31270185insAAGCA , CM000668.2:g.31270184_31270185insAAGCA GRCh38
NC_000006.11:g.31237961_31237962insAAGCA , CM000668.1:g.31237961_31237962insAAGCA GRCh37
NC_000006.10:g.31345940_31345941insAAGCA NCBI36
NG_029422.2:g.6948_6949insGCTTT

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.895+26_895+27insGCTTT MANE Select ENSP00000365402.5:n.895+26_895+27insGCTTT
ENST00000376228.9:c.895+26_895+27insGCTTT ENSP00000365402.5:n.895+26_895+27insGCTTT
ENST00000376237.8:c.*482+26_*482+27insGCTTT ENSP00000365412.4:n.*482+26_*482+27insGCTTT
ENST00000383329.7:c.895+26_895+27insGCTTT ENSP00000372819.3:n.895+26_895+27insGCTTT
ENST00000470363.5:n.213+26_213+27insGCTTT
ENST00000487245.5:n.1254+26_1254+27insGCTTT
NM_002117.5:c.895+26_895+27insGCTTT NP_002108.4:n.895+26_895+27insGCTTT
NM_002117.6:c.895+26_895+27insGCTTT MANE Select NP_002108.4:n.895+26_895+27insGCTTT