Canonical Allele Identifier: CA2677950285
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269988_31269989insTCA , CM000668.2:g.31269988_31269989insTCA GRCh38
NC_000006.11:g.31237765_31237766insTCA , CM000668.1:g.31237765_31237766insTCA GRCh37
NC_000006.10:g.31345744_31345745insTCA NCBI36
NG_029422.2:g.7143_7144insTGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.992_993insTGA MANE Select ENSP00000365402.5:p.Met331delinsIleGlu
ENST00000376228.9:c.992_993insTGA ENSP00000365402.5:p.Met331delinsIleGlu
ENST00000376237.8:c.*579_*580insTGA ENSP00000365412.4:n.*579_*580insTGA
ENST00000383329.7:c.992_993insTGA ENSP00000372819.3:p.Met331delinsIleGlu
ENST00000470363.5:n.310_311insTGA
ENST00000487245.5:n.1351_1352insTGA
NM_002117.5:c.992_993insTGA NP_002108.4:p.Met331delinsIleGlu
NM_002117.6:c.992_993insTGA MANE Select NP_002108.4:p.Met331delinsIleGlu