Canonical Allele Identifier: CA2375067844
Gene: DNAJC5 HGNC NCBI

Linked Data

dbSNP Id: rs1600891143

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63933324T>G , CM000682.2:g.63933324T>G GRCh38
NC_000020.10:g.62564677T>G , CM000682.1:g.62564677T>G GRCh37
NC_000020.9:g.62035121T>G NCBI36
NG_029805.1:g.43223T>G
NG_029805.2:g.43223T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000703637.1:c.*1923T>G ENSP00000515413.1:n.*1923T>G
ENST00000360864.9:c.*1756T>G MANE Select ENSP00000354111.4:n.*1756T>G
ENST00000360864.8:c.*1756T>G ENSP00000354111.4:n.*1756T>G
ENST00000470551.1:c.*1923T>G ENSP00000434744.1:n.*1923T>G
NM_025219.2:c.*1756T>G NP_079495.1:n.*1756T>G
XM_011529048.1:c.*1756T>G XP_011527350.1:n.*1756T>G
XM_011529049.1:c.*1756T>G XP_011527351.1:n.*1756T>G
XM_011529050.1:c.*1756T>G XP_011527352.1:n.*1756T>G
XR_936629.1:n.3059T>G
XR_936630.1:n.3317T>G
XM_011529048.2:c.*1756T>G XP_011527350.1:n.*1756T>G
XR_936629.2:n.3072T>G
NM_025219.3:c.*1756T>G MANE Select NP_079495.1:n.*1756T>G