Canonical Allele Identifier: CA2375067853
Gene: DNAJC5 HGNC NCBI

Linked Data

dbSNP Id: rs2053690188

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63933336T>C , CM000682.2:g.63933336T>C GRCh38
NC_000020.10:g.62564689T>C , CM000682.1:g.62564689T>C GRCh37
NC_000020.9:g.62035133T>C NCBI36
NG_029805.1:g.43235T>C
NG_029805.2:g.43235T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000703637.1:c.*1935T>C ENSP00000515413.1:n.*1935T>C
ENST00000360864.9:c.*1768T>C MANE Select ENSP00000354111.4:n.*1768T>C
ENST00000360864.8:c.*1768T>C ENSP00000354111.4:n.*1768T>C
ENST00000470551.1:c.*1935T>C ENSP00000434744.1:n.*1935T>C
NM_025219.2:c.*1768T>C NP_079495.1:n.*1768T>C
XM_011529048.1:c.*1768T>C XP_011527350.1:n.*1768T>C
XM_011529049.1:c.*1768T>C XP_011527351.1:n.*1768T>C
XM_011529050.1:c.*1768T>C XP_011527352.1:n.*1768T>C
XR_936629.1:n.3071T>C
XR_936630.1:n.3329T>C
XM_011529048.2:c.*1768T>C XP_011527350.1:n.*1768T>C
XR_936629.2:n.3084T>C
NM_025219.3:c.*1768T>C MANE Select NP_079495.1:n.*1768T>C