Canonical Allele Identifier: CA2653894189

Gene: DNAJC5

Linked Data

• gnomAD v4: 20-63930778-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63930778G>T , CM000682.2:g.63930778G>T	GRCh38
NC_000020.10:g.62562131G>T , CM000682.1:g.62562131G>T	GRCh37
NC_000020.9:g.62032575G>T	NCBI36
NG_029805.1:g.40677G>T
NG_029805.2:g.40677G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000703637.1:c.322-73G>T	ENSP00000515413.1:n.322-73G>T
ENST00000360864.9:c.322-73G>T MANE Select	ENSP00000354111.4:n.322-73G>T
ENST00000360864.8:c.322-73G>T	ENSP00000354111.4:n.322-73G>T
ENST00000470551.1:c.322-73G>T	ENSP00000434744.1:n.322-73G>T
NM_025219.2:c.322-73G>T	NP_079495.1:n.322-73G>T
XM_011529048.1:c.322-73G>T	XP_011527350.1:n.322-73G>T
XM_011529049.1:c.322-73G>T	XP_011527351.1:n.322-73G>T
XM_011529050.1:c.322-73G>T	XP_011527352.1:n.322-73G>T
XR_936629.1:n.954-73G>T
XR_936630.1:n.1212-73G>T
XM_011529048.2:c.322-73G>T	XP_011527350.1:n.322-73G>T
XR_936629.2:n.967-73G>T
NM_025219.3:c.322-73G>T MANE Select	NP_079495.1:n.322-73G>T