Canonical Allele Identifier: CA2677951287
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271159_31271170del , CM000668.2:g.31271159_31271170del GRCh38
NC_000006.11:g.31238936_31238947del , CM000668.1:g.31238936_31238947del GRCh37
NC_000006.10:g.31346915_31346926del NCBI36
NG_029422.2:g.5962_5973del

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.522_533del MANE Select ENSP00000365402.5:p.Arg175_Glu178del
ENST00000376228.9:c.522_533del ENSP00000365402.5:p.Arg175_Glu178del
ENST00000376237.8:c.*109_*120del ENSP00000365412.4:n.*109_*120del
ENST00000383329.7:c.522_533del ENSP00000372819.3:p.Arg175_Glu178del
ENST00000415537.1:c.520_531del
ENST00000484378.1:n.791_802del
ENST00000487245.5:n.881_892del
ENST00000495835.1:n.711_722del
NM_002117.5:c.522_533del NP_002108.4:p.Arg175_Glu178del
NM_002117.6:c.522_533del MANE Select NP_002108.4:p.Arg175_Glu178del