Canonical Allele Identifier: CA2737103564
Gene: DNAJC5 HGNC NCBI

Linked Data

dbSNP Id: rs2146312090

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63933268_63933277del , CM000682.2:g.63933268_63933277del GRCh38
NC_000020.10:g.62564621_62564630del , CM000682.1:g.62564621_62564630del GRCh37
NC_000020.9:g.62035065_62035074del NCBI36
NG_029805.1:g.43167_43176del
NG_029805.2:g.43167_43176del

Transcript Alleles

HGVS Amino-acid Change
ENST00000703637.1:c.*1867_*1876del ENSP00000515413.1:n.*1867_*1876del
ENST00000360864.9:c.*1700_*1709del MANE Select ENSP00000354111.4:n.*1700_*1709del
ENST00000360864.8:c.*1700_*1709del ENSP00000354111.4:n.*1700_*1709del
ENST00000470551.1:c.*1867_*1876del ENSP00000434744.1:n.*1867_*1876del
NM_025219.2:c.*1700_*1709del NP_079495.1:n.*1700_*1709del
XM_011529048.1:c.*1700_*1709del XP_011527350.1:n.*1700_*1709del
XM_011529049.1:c.*1700_*1709del XP_011527351.1:n.*1700_*1709del
XM_011529050.1:c.*1700_*1709del XP_011527352.1:n.*1700_*1709del
XR_936629.1:n.3003_3012del
XR_936630.1:n.3261_3270del
XM_011529048.2:c.*1700_*1709del XP_011527350.1:n.*1700_*1709del
XR_936629.2:n.3016_3025del
NM_025219.3:c.*1700_*1709del MANE Select NP_079495.1:n.*1700_*1709del