Canonical Allele Identifier: CA2677951466
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271429_31271432del , CM000668.2:g.31271429_31271432del GRCh38
NC_000006.11:g.31239206_31239209del , CM000668.1:g.31239206_31239209del GRCh37
NC_000006.10:g.31347185_31347188del NCBI36
NG_029422.2:g.5700_5703del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.344-84_344-81del MANE Select ENSP00000365402.5:n.344-84_344-81del
ENST00000376228.9:c.344-84_344-81del ENSP00000365402.5:n.344-84_344-81del
ENST00000376237.8:c.344-101_344-98del ENSP00000365412.4:n.344-101_344-98del
ENST00000383329.7:c.344-84_344-81del ENSP00000372819.3:n.344-84_344-81del
ENST00000415537.1:c.342-84_342-81del
ENST00000484378.1:n.529_532del
ENST00000487245.5:n.619_622del
ENST00000495835.1:n.533-84_533-81del
NM_002117.5:c.344-84_344-81del NP_002108.4:n.344-84_344-81del
NM_002117.6:c.344-84_344-81del MANE Select NP_002108.4:n.344-84_344-81del