Canonical Allele Identifier: CA746503332

Gene: DNAJC5

Linked Data

• dbSNP Id: rs1353700467
• gnomAD v3: 20-63933110-A-AG
• gnomAD v4: 20-63933110-A-AG
• MyVariant Identifiers: chr20:g.62564463_62564464insG (hg19) ; chr20:g.63933110_63933111insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63933112dup , CM000682.2:g.63933112dup	GRCh38
NC_000020.10:g.62564465dup , CM000682.1:g.62564465dup	GRCh37
NC_000020.9:g.62034909dup	NCBI36
NG_029805.1:g.43011dup
NG_029805.2:g.43011dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703637.1:c.*1711dup	ENSP00000515413.1:n.*1711dup
ENST00000360864.9:c.*1544dup MANE Select	ENSP00000354111.4:n.*1544dup
ENST00000360864.8:c.*1544dup	ENSP00000354111.4:n.*1544dup
ENST00000470551.1:c.*1711dup	ENSP00000434744.1:n.*1711dup
NM_025219.2:c.*1544dup	NP_079495.1:n.*1544dup
XM_011529048.1:c.*1544dup	XP_011527350.1:n.*1544dup
XM_011529049.1:c.*1544dup	XP_011527351.1:n.*1544dup
XM_011529050.1:c.*1544dup	XP_011527352.1:n.*1544dup
XR_936629.1:n.2847dup
XR_936630.1:n.3105dup
XM_011529048.2:c.*1544dup	XP_011527350.1:n.*1544dup
XR_936629.2:n.2860dup
NM_025219.3:c.*1544dup MANE Select	NP_079495.1:n.*1544dup