Canonical Allele Identifier: CA2653896135

Gene: DNAJC5

Linked Data

• gnomAD v4: 20-63933063-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63933063G>T , CM000682.2:g.63933063G>T	GRCh38
NC_000020.10:g.62564416G>T , CM000682.1:g.62564416G>T	GRCh37
NC_000020.9:g.62034860G>T	NCBI36
NG_029805.1:g.42962G>T
NG_029805.2:g.42962G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703637.1:c.*1662G>T	ENSP00000515413.1:n.*1662G>T
ENST00000360864.9:c.*1495G>T MANE Select	ENSP00000354111.4:n.*1495G>T
ENST00000360864.8:c.*1495G>T	ENSP00000354111.4:n.*1495G>T
ENST00000470551.1:c.*1662G>T	ENSP00000434744.1:n.*1662G>T
NM_025219.2:c.*1495G>T	NP_079495.1:n.*1495G>T
XM_011529048.1:c.*1495G>T	XP_011527350.1:n.*1495G>T
XM_011529049.1:c.*1495G>T	XP_011527351.1:n.*1495G>T
XM_011529050.1:c.*1495G>T	XP_011527352.1:n.*1495G>T
XR_936629.1:n.2798G>T
XR_936630.1:n.3056G>T
XM_011529048.2:c.*1495G>T	XP_011527350.1:n.*1495G>T
XR_936629.2:n.2811G>T
NM_025219.3:c.*1495G>T MANE Select	NP_079495.1:n.*1495G>T