Canonical Allele Identifier: CA917584513
Gene: UQCRQ HGNC NCBI

Linked Data

dbSNP Id: rs1554072238

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132868758_132868760del , CM000667.2:g.132868758_132868760del GRCh38
NC_000005.9:g.132204450_132204452del , CM000667.1:g.132204450_132204452del GRCh37
NC_000005.8:g.132232349_132232351del NCBI36
NG_012221.1:g.7132_7134del
NG_047051.1:g.3128_3130del

Transcript Alleles

HGVS Amino-acid Change
ENST00000378670.8:c.*1176_*1178del MANE Select ENSP00000367939.3:n.*1176_*1178del
NM_014402.4:c.*1176_*1178del NP_055217.2:n.*1176_*1178del
NM_014402.5:c.*1176_*1178del MANE Select NP_055217.2:n.*1176_*1178del