Canonical Allele Identifier: CA10644426

Gene: DNAJC5

Linked Data

• ClinVar Variation Id: 339432
• ClinVar RCV Id: RCV000397074 ; RCV001142014
• dbSNP Id: rs77107548
• gnomAD v2: 20-62566591-A-G
• gnomAD v3: 20-63935238-A-G
• gnomAD v4: 20-63935238-A-G
• MyVariant Identifiers: chr20:g.62566591A>G (hg19) ; chr20:g.62566591_62566594delinsGTGC (hg19) ; chr20:g.63935238A>G (hg38) ; chr20:g.63935238_63935241delinsGTGC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63935238A>G , CM000682.2:g.63935238A>G	GRCh38
NC_000020.10:g.62566591A>G , CM000682.1:g.62566591A>G	GRCh37
NC_000020.9:g.62037035A>G	NCBI36
NG_029805.1:g.45137A>G
NG_029805.2:g.45137A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360864.9:c.*3670A>G MANE Select	ENSP00000354111.4:n.*3670A>G
ENST00000360864.8:c.*3670A>G	ENSP00000354111.4:n.*3670A>G
ENST00000470551.1:c.*3837A>G	ENSP00000434744.1:n.*3837A>G
NM_025219.2:c.*3670A>G	NP_079495.1:n.*3670A>G
XM_011529048.1:c.*3670A>G	XP_011527350.1:n.*3670A>G
XM_011529049.1:c.*3670A>G	XP_011527351.1:n.*3670A>G
XM_011529050.1:c.*3670A>G	XP_011527352.1:n.*3670A>G
XR_936629.1:n.4973A>G
XR_936630.1:n.5231A>G
XM_011529048.2:c.*3670A>G	XP_011527350.1:n.*3670A>G
XR_936629.2:n.4986A>G
NM_025219.3:c.*3670A>G MANE Select	NP_079495.1:n.*3670A>G