Canonical Allele Identifier: CA317525181

Gene: DNAJC5

Linked Data

• dbSNP Id: rs954961042
• gnomAD v2: 20-62564709-AG-A
• gnomAD v3: 20-63933356-AG-A
• gnomAD v4: 20-63933356-AG-A
• MyVariant Identifiers: chr20:g.62564710del (hg19) ; chr20:g.63933357del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63933359del , CM000682.2:g.63933359del	GRCh38
NC_000020.10:g.62564712del , CM000682.1:g.62564712del	GRCh37
NC_000020.9:g.62035156del	NCBI36
NG_029805.1:g.43258del
NG_029805.2:g.43258del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703637.1:c.*1958del	ENSP00000515413.1:n.*1958del
ENST00000360864.9:c.*1791del MANE Select	ENSP00000354111.4:n.*1791del
ENST00000360864.8:c.*1791del	ENSP00000354111.4:n.*1791del
ENST00000470551.1:c.*1958del	ENSP00000434744.1:n.*1958del
NM_025219.2:c.*1791del	NP_079495.1:n.*1791del
XM_011529048.1:c.*1791del	XP_011527350.1:n.*1791del
XM_011529049.1:c.*1791del	XP_011527351.1:n.*1791del
XM_011529050.1:c.*1791del	XP_011527352.1:n.*1791del
XR_936629.1:n.3094del
XR_936630.1:n.3352del
XM_011529048.2:c.*1791del	XP_011527350.1:n.*1791del
XR_936629.2:n.3107del
NM_025219.3:c.*1791del MANE Select	NP_079495.1:n.*1791del