Canonical Allele Identifier: CA317525180

Gene: DNAJC5

Linked Data

• dbSNP Id: rs1029379078
• gnomAD v3: 20-63933333-G-A
• gnomAD v4: 20-63933333-G-A
• MyVariant Identifiers: chr20:g.62564686G>A (hg19) ; chr20:g.63933333G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63933333G>A , CM000682.2:g.63933333G>A	GRCh38
NC_000020.10:g.62564686G>A , CM000682.1:g.62564686G>A	GRCh37
NC_000020.9:g.62035130G>A	NCBI36
NG_029805.1:g.43232G>A
NG_029805.2:g.43232G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703637.1:c.*1932G>A	ENSP00000515413.1:n.*1932G>A
ENST00000360864.9:c.*1765G>A MANE Select	ENSP00000354111.4:n.*1765G>A
ENST00000360864.8:c.*1765G>A	ENSP00000354111.4:n.*1765G>A
ENST00000470551.1:c.*1932G>A	ENSP00000434744.1:n.*1932G>A
NM_025219.2:c.*1765G>A	NP_079495.1:n.*1765G>A
XM_011529048.1:c.*1765G>A	XP_011527350.1:n.*1765G>A
XM_011529049.1:c.*1765G>A	XP_011527351.1:n.*1765G>A
XM_011529050.1:c.*1765G>A	XP_011527352.1:n.*1765G>A
XR_936629.1:n.3068G>A
XR_936630.1:n.3326G>A
XM_011529048.2:c.*1765G>A	XP_011527350.1:n.*1765G>A
XR_936629.2:n.3081G>A
NM_025219.3:c.*1765G>A MANE Select	NP_079495.1:n.*1765G>A