Canonical Allele Identifier: CA1019329454

Gene: DNAJC5

Linked Data

• dbSNP Id: rs2053690005
• gnomAD v3: 20-63933323-A-T
• gnomAD v4: 20-63933323-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63933323A>T , CM000682.2:g.63933323A>T	GRCh38
NC_000020.10:g.62564676A>T , CM000682.1:g.62564676A>T	GRCh37
NC_000020.9:g.62035120A>T	NCBI36
NG_029805.1:g.43222A>T
NG_029805.2:g.43222A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703637.1:c.*1922A>T	ENSP00000515413.1:n.*1922A>T
ENST00000360864.9:c.*1755A>T MANE Select	ENSP00000354111.4:n.*1755A>T
ENST00000360864.8:c.*1755A>T	ENSP00000354111.4:n.*1755A>T
ENST00000470551.1:c.*1922A>T	ENSP00000434744.1:n.*1922A>T
NM_025219.2:c.*1755A>T	NP_079495.1:n.*1755A>T
XM_011529048.1:c.*1755A>T	XP_011527350.1:n.*1755A>T
XM_011529049.1:c.*1755A>T	XP_011527351.1:n.*1755A>T
XM_011529050.1:c.*1755A>T	XP_011527352.1:n.*1755A>T
XR_936629.1:n.3058A>T
XR_936630.1:n.3316A>T
XM_011529048.2:c.*1755A>T	XP_011527350.1:n.*1755A>T
XR_936629.2:n.3071A>T
NM_025219.3:c.*1755A>T MANE Select	NP_079495.1:n.*1755A>T