Canonical Allele Identifier: CA136862992
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs796547294
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270183_31270188delinsCACATC , CM000668.2:g.31270183_31270188delinsCACATC GRCh38
NC_000006.11:g.31237960_31237965delinsCACATC , CM000668.1:g.31237960_31237965delinsCACATC GRCh37
NC_000006.10:g.31345939_31345944delinsCACATC NCBI36
NG_029422.2:g.6944_6949delinsGATGTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.895+22_895+27delinsGATGTG MANE Select ENSP00000365402.5:n.895+22_895+27delinsGATGTG
ENST00000376228.9:c.895+22_895+27delinsGATGTG ENSP00000365402.5:n.895+22_895+27delinsGATGTG
ENST00000376237.8:c.*482+22_*482+27delinsGATGTG ENSP00000365412.4:n.*482+22_*482+27delinsGATGTG
ENST00000383329.7:c.895+22_895+27delinsGATGTG ENSP00000372819.3:n.895+22_895+27delinsGATGTG
ENST00000470363.5:n.213+22_213+27delinsGATGTG
ENST00000487245.5:n.1254+22_1254+27delinsGATGTG
NM_002117.5:c.895+22_895+27delinsGATGTG NP_002108.4:n.895+22_895+27delinsGATGTG
NM_002117.6:c.895+22_895+27delinsGATGTG MANE Select NP_002108.4:n.895+22_895+27delinsGATGTG
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