Canonical Allele Identifier: CA746503638

Gene: DNAJC5

Linked Data

• dbSNP Id: rs1195263516
• gnomAD v3: 20-63933329-A-G
• gnomAD v4: 20-63933329-A-G
• MyVariant Identifiers: chr20:g.62564682A>G (hg19) ; chr20:g.63933329A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63933329A>G , CM000682.2:g.63933329A>G	GRCh38
NC_000020.10:g.62564682A>G , CM000682.1:g.62564682A>G	GRCh37
NC_000020.9:g.62035126A>G	NCBI36
NG_029805.1:g.43228A>G
NG_029805.2:g.43228A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703637.1:c.*1928A>G	ENSP00000515413.1:n.*1928A>G
ENST00000360864.9:c.*1761A>G MANE Select	ENSP00000354111.4:n.*1761A>G
ENST00000360864.8:c.*1761A>G	ENSP00000354111.4:n.*1761A>G
ENST00000470551.1:c.*1928A>G	ENSP00000434744.1:n.*1928A>G
NM_025219.2:c.*1761A>G	NP_079495.1:n.*1761A>G
XM_011529048.1:c.*1761A>G	XP_011527350.1:n.*1761A>G
XM_011529049.1:c.*1761A>G	XP_011527351.1:n.*1761A>G
XM_011529050.1:c.*1761A>G	XP_011527352.1:n.*1761A>G
XR_936629.1:n.3064A>G
XR_936630.1:n.3322A>G
XM_011529048.2:c.*1761A>G	XP_011527350.1:n.*1761A>G
XR_936629.2:n.3077A>G
NM_025219.3:c.*1761A>G MANE Select	NP_079495.1:n.*1761A>G