Canonical Allele Identifier: CA317525018

Gene: DNAJC5

Linked Data

• dbSNP Id: rs773078929
• gnomAD v3: 20-63933141-G-T
• gnomAD v4: 20-63933141-G-T
• MyVariant Identifiers: chr20:g.62564494G>T (hg19) ; chr20:g.63933141G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63933141G>T , CM000682.2:g.63933141G>T	GRCh38
NC_000020.10:g.62564494G>T , CM000682.1:g.62564494G>T	GRCh37
NC_000020.9:g.62034938G>T	NCBI36
NG_029805.1:g.43040G>T
NG_029805.2:g.43040G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703637.1:c.*1740G>T	ENSP00000515413.1:n.*1740G>T
ENST00000360864.9:c.*1573G>T MANE Select	ENSP00000354111.4:n.*1573G>T
ENST00000360864.8:c.*1573G>T	ENSP00000354111.4:n.*1573G>T
ENST00000470551.1:c.*1740G>T	ENSP00000434744.1:n.*1740G>T
NM_025219.2:c.*1573G>T	NP_079495.1:n.*1573G>T
XM_011529048.1:c.*1573G>T	XP_011527350.1:n.*1573G>T
XM_011529049.1:c.*1573G>T	XP_011527351.1:n.*1573G>T
XM_011529050.1:c.*1573G>T	XP_011527352.1:n.*1573G>T
XR_936629.1:n.2876G>T
XR_936630.1:n.3134G>T
XM_011529048.2:c.*1573G>T	XP_011527350.1:n.*1573G>T
XR_936629.2:n.2889G>T
NM_025219.3:c.*1573G>T MANE Select	NP_079495.1:n.*1573G>T