Canonical Allele Identifier: CA1019328159
Gene: DNAJC5 HGNC NCBI

Linked Data

dbSNP Id: rs2053662426

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63930786G>A , CM000682.2:g.63930786G>A GRCh38
NC_000020.10:g.62562139G>A , CM000682.1:g.62562139G>A GRCh37
NC_000020.9:g.62032583G>A NCBI36
NG_029805.1:g.40685G>A
NG_029805.2:g.40685G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000703637.1:c.322-65G>A ENSP00000515413.1:n.322-65G>A
ENST00000360864.9:c.322-65G>A MANE Select ENSP00000354111.4:n.322-65G>A
ENST00000360864.8:c.322-65G>A ENSP00000354111.4:n.322-65G>A
ENST00000470551.1:c.322-65G>A ENSP00000434744.1:n.322-65G>A
NM_025219.2:c.322-65G>A NP_079495.1:n.322-65G>A
XM_011529048.1:c.322-65G>A XP_011527350.1:n.322-65G>A
XM_011529049.1:c.322-65G>A XP_011527351.1:n.322-65G>A
XM_011529050.1:c.322-65G>A XP_011527352.1:n.322-65G>A
XR_936629.1:n.954-65G>A
XR_936630.1:n.1212-65G>A
XM_011529048.2:c.322-65G>A XP_011527350.1:n.322-65G>A
XR_936629.2:n.967-65G>A
NM_025219.3:c.322-65G>A MANE Select NP_079495.1:n.322-65G>A