Canonical Allele Identifier: CA2375066497
Gene: DNAJC5 HGNC NCBI

Linked Data

dbSNP Id: rs2053662311

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63930781T>C , CM000682.2:g.63930781T>C GRCh38
NC_000020.10:g.62562134T>C , CM000682.1:g.62562134T>C GRCh37
NC_000020.9:g.62032578T>C NCBI36
NG_029805.1:g.40680T>C
NG_029805.2:g.40680T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000703637.1:c.322-70T>C ENSP00000515413.1:n.322-70T>C
ENST00000360864.9:c.322-70T>C MANE Select ENSP00000354111.4:n.322-70T>C
ENST00000360864.8:c.322-70T>C ENSP00000354111.4:n.322-70T>C
ENST00000470551.1:c.322-70T>C ENSP00000434744.1:n.322-70T>C
NM_025219.2:c.322-70T>C NP_079495.1:n.322-70T>C
XM_011529048.1:c.322-70T>C XP_011527350.1:n.322-70T>C
XM_011529049.1:c.322-70T>C XP_011527351.1:n.322-70T>C
XM_011529050.1:c.322-70T>C XP_011527352.1:n.322-70T>C
XR_936629.1:n.954-70T>C
XR_936630.1:n.1212-70T>C
XM_011529048.2:c.322-70T>C XP_011527350.1:n.322-70T>C
XR_936629.2:n.967-70T>C
NM_025219.3:c.322-70T>C MANE Select NP_079495.1:n.322-70T>C