Canonical Allele Identifier: CA2677949835
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269577_31269581del , CM000668.2:g.31269577_31269581del GRCh38
NC_000006.11:g.31237354_31237358del , CM000668.1:g.31237354_31237358del GRCh37
NC_000006.10:g.31345333_31345337del NCBI36
NG_029422.2:g.7552_7556del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1016-55_1016-51del MANE Select ENSP00000365402.5:n.1016-55_1016-51del
ENST00000376228.9:c.1016-55_1016-51del ENSP00000365402.5:n.1016-55_1016-51del
ENST00000376237.8:c.*603-55_*603-51del ENSP00000365412.4:n.*603-55_*603-51del
ENST00000383329.7:c.1016-37_1016-33del ENSP00000372819.3:n.1016-37_1016-33del
ENST00000466892.5:n.87_91del
ENST00000470363.5:n.719_723del
ENST00000487245.5:n.1375-55_1375-51del
NM_002117.5:c.1016-55_1016-51del NP_002108.4:n.1016-55_1016-51del
NM_002117.6:c.1016-55_1016-51del MANE Select NP_002108.4:n.1016-55_1016-51del