Canonical Allele Identifier: CA2375067820
Gene: DNAJC5 HGNC NCBI

Linked Data

dbSNP Id: rs1568992153

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63933283G>C , CM000682.2:g.63933283G>C GRCh38
NC_000020.10:g.62564636G>C , CM000682.1:g.62564636G>C GRCh37
NC_000020.9:g.62035080G>C NCBI36
NG_029805.1:g.43182G>C
NG_029805.2:g.43182G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000703637.1:c.*1882G>C ENSP00000515413.1:n.*1882G>C
ENST00000360864.9:c.*1715G>C MANE Select ENSP00000354111.4:n.*1715G>C
ENST00000360864.8:c.*1715G>C ENSP00000354111.4:n.*1715G>C
ENST00000470551.1:c.*1882G>C ENSP00000434744.1:n.*1882G>C
NM_025219.2:c.*1715G>C NP_079495.1:n.*1715G>C
XM_011529048.1:c.*1715G>C XP_011527350.1:n.*1715G>C
XM_011529049.1:c.*1715G>C XP_011527351.1:n.*1715G>C
XM_011529050.1:c.*1715G>C XP_011527352.1:n.*1715G>C
XR_936629.1:n.3018G>C
XR_936630.1:n.3276G>C
XM_011529048.2:c.*1715G>C XP_011527350.1:n.*1715G>C
XR_936629.2:n.3031G>C
NM_025219.3:c.*1715G>C MANE Select NP_079495.1:n.*1715G>C