Canonical Allele Identifier: CA2677951549
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271493_31271497del , CM000668.2:g.31271493_31271497del GRCh38
NC_000006.11:g.31239270_31239274del , CM000668.1:g.31239270_31239274del GRCh37
NC_000006.10:g.31347249_31347253del NCBI36
NG_029422.2:g.5635_5639del

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.343+102_343+106del MANE Select ENSP00000365402.5:n.343+102_343+106del
ENST00000376228.9:c.343+102_343+106del ENSP00000365402.5:n.343+102_343+106del
ENST00000376237.8:c.343+102_343+106del ENSP00000365412.4:n.343+102_343+106del
ENST00000383329.7:c.343+102_343+106del ENSP00000372819.3:n.343+102_343+106del
ENST00000415537.1:c.341+102_341+106del
ENST00000484378.1:n.464_468del
ENST00000487245.5:n.554_558del
ENST00000495835.1:n.532+102_532+106del
NM_002117.5:c.343+102_343+106del NP_002108.4:n.343+102_343+106del
NM_002117.6:c.343+102_343+106del MANE Select NP_002108.4:n.343+102_343+106del