Canonical Allele Identifier: CA1619078858
Gene: HLA-C HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270039_31270085delinsGCCAGCAACGATGCCCATGATGGGGATGGTGGGCTGGGAAGATGGCT , CM000668.2:g.31270039_31270085delinsGCCAGCAACGATGCCCATGATGGGGATGGTGGGCTGGGAAGATGGCT GRCh38
NC_000006.11:g.31237816_31237862delinsGCCAGCAACGATGCCCATGATGGGGATGGTGGGCTGGGAAGATGGCT , CM000668.1:g.31237816_31237862delinsGCCAGCAACGATGCCCATGATGGGGATGGTGGGCTGGGAAGATGGCT GRCh37
NC_000006.10:g.31345795_31345841delinsGCCAGCAACGATGCCCATGATGGGGATGGTGGGCTGGGAAGATGGCT NCBI36
NG_029422.2:g.7047_7093delinsAGCCATCTTCCCAGCCCACCATCCCCATCATGGGCATCGTTGCTGGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.896_942delinsAGCCATCTTCCCAGCCCACCATCCCCATCATGGGCATCGTTGCTGGC MANE Select ENSP00000365402.5:p.Glu299=
ENST00000376228.9:c.896_942delinsAGCCATCTTCCCAGCCCACCATCCCCATCATGGGCATCGTTGCTGGC ENSP00000365402.5:p.Glu299=
ENST00000376237.8:c.*483_*529delinsAGCCATCTTCCCAGCCCACCATCCCCATCATGGGCATCGTTGCTGGC ENSP00000365412.4:n.*483_*529delinsAGCCATCTTCCCAGCCCACCATCCCC...
ENST00000383329.7:c.896_942delinsAGCCATCTTCCCAGCCCACCATCCCCATCATGGGCATCGTTGCTGGC ENSP00000372819.3:p.Glu299=
ENST00000470363.5:n.214_260delinsAGCCATCTTCCCAGCCCACCATCCCCATCATGGGCATCGTTGCTGGC
ENST00000487245.5:n.1255_1301delinsAGCCATCTTCCCAGCCCACCATCCCCATCATGGGCATCGTTGCTGGC
NM_002117.5:c.896_942delinsAGCCATCTTCCCAGCCCACCATCCCCATCATGGGCATCGTTGCTGGC NP_002108.4:p.Glu299=
NM_002117.6:c.896_942delinsAGCCATCTTCCCAGCCCACCATCCCCATCATGGGCATCGTTGCTGGC MANE Select NP_002108.4:p.Glu299=
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