Canonical Allele Identifier: CA2595999825

Gene: DNAJC5

Linked Data

• dbSNP Id: rs2146312108
• gnomAD v3: 20-63933277-C-CA
• gnomAD v4: 20-63933277-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63933278dup , CM000682.2:g.63933278dup	GRCh38
NC_000020.10:g.62564631dup , CM000682.1:g.62564631dup	GRCh37
NC_000020.9:g.62035075dup	NCBI36
NG_029805.1:g.43177dup
NG_029805.2:g.43177dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703637.1:c.*1877dup	ENSP00000515413.1:n.*1877dup
ENST00000360864.9:c.*1710dup MANE Select	ENSP00000354111.4:n.*1710dup
ENST00000360864.8:c.*1710dup	ENSP00000354111.4:n.*1710dup
ENST00000470551.1:c.*1877dup	ENSP00000434744.1:n.*1877dup
NM_025219.2:c.*1710dup	NP_079495.1:n.*1710dup
XM_011529048.1:c.*1710dup	XP_011527350.1:n.*1710dup
XM_011529049.1:c.*1710dup	XP_011527351.1:n.*1710dup
XM_011529050.1:c.*1710dup	XP_011527352.1:n.*1710dup
XR_936629.1:n.3013dup
XR_936630.1:n.3271dup
XM_011529048.2:c.*1710dup	XP_011527350.1:n.*1710dup
XR_936629.2:n.3026dup
NM_025219.3:c.*1710dup MANE Select	NP_079495.1:n.*1710dup