Canonical Allele Identifier: CA2677950283
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269988_31269989insGCA , CM000668.2:g.31269988_31269989insGCA GRCh38
NC_000006.11:g.31237765_31237766insGCA , CM000668.1:g.31237765_31237766insGCA GRCh37
NC_000006.10:g.31345744_31345745insGCA NCBI36
NG_029422.2:g.7143_7144insTGC

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.992_993insTGC MANE Select ENSP00000365402.5:p.Met331delinsIleAla
ENST00000376228.9:c.992_993insTGC ENSP00000365402.5:p.Met331delinsIleAla
ENST00000376237.8:c.*579_*580insTGC ENSP00000365412.4:n.*579_*580insTGC
ENST00000383329.7:c.992_993insTGC ENSP00000372819.3:p.Met331delinsIleAla
ENST00000470363.5:n.310_311insTGC
ENST00000487245.5:n.1351_1352insTGC
NM_002117.5:c.992_993insTGC NP_002108.4:p.Met331delinsIleAla
NM_002117.6:c.992_993insTGC MANE Select NP_002108.4:p.Met331delinsIleAla