Canonical Allele Identifier: CA746503688

Gene: DNAJC5

Linked Data

• dbSNP Id: rs1205527688
• MyVariant Identifiers: chr20:g.62564781_62564782insAGCT (hg19) ; chr20:g.63933428_63933429insAGCT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63933429_63933432dup , CM000682.2:g.63933429_63933432dup	GRCh38
NC_000020.10:g.62564782_62564785dup , CM000682.1:g.62564782_62564785dup	GRCh37
NC_000020.9:g.62035226_62035229dup	NCBI36
NG_029805.1:g.43328_43331dup
NG_029805.2:g.43328_43331dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703637.1:c.*2028_*2031dup	ENSP00000515413.1:n.*2028_*2031dup
ENST00000360864.9:c.*1861_*1864dup MANE Select	ENSP00000354111.4:n.*1861_*1864dup
ENST00000360864.8:c.*1861_*1864dup	ENSP00000354111.4:n.*1861_*1864dup
ENST00000470551.1:c.*2028_*2031dup	ENSP00000434744.1:n.*2028_*2031dup
NM_025219.2:c.*1861_*1864dup	NP_079495.1:n.*1861_*1864dup
XM_011529048.1:c.*1861_*1864dup	XP_011527350.1:n.*1861_*1864dup
XM_011529049.1:c.*1861_*1864dup	XP_011527351.1:n.*1861_*1864dup
XM_011529050.1:c.*1861_*1864dup	XP_011527352.1:n.*1861_*1864dup
XR_936629.1:n.3164_3167dup
XR_936630.1:n.3422_3425dup
XM_011529048.2:c.*1861_*1864dup	XP_011527350.1:n.*1861_*1864dup
XR_936629.2:n.3177_3180dup
NM_025219.3:c.*1861_*1864dup MANE Select	NP_079495.1:n.*1861_*1864dup