Canonical Allele Identifier: CA10644409
Gene: DNAJC5 HGNC NCBI

Linked Data

ClinVar Variation Id: 339411
ClinVar RCV Id: RCV000353528 RCV001143709 RCV001683353
dbSNP Id: rs11554628
gnomAD v2: 20-62565646-G-A
gnomAD v3: 20-63934293-G-A
gnomAD v4: 20-63934293-G-A
MyVariant Identifiers: chr20:g.62565646G>A (hg19) chr20:g.63934293G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63934293G>A , CM000682.2:g.63934293G>A GRCh38
NC_000020.10:g.62565646G>A , CM000682.1:g.62565646G>A GRCh37
NC_000020.9:g.62036090G>A NCBI36
NG_029805.1:g.44192G>A
NG_029805.2:g.44192G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360864.9:c.*2725G>A MANE Select ENSP00000354111.4:n.*2725G>A
ENST00000360864.8:c.*2725G>A ENSP00000354111.4:n.*2725G>A
ENST00000470551.1:c.*2892G>A ENSP00000434744.1:n.*2892G>A
NM_025219.2:c.*2725G>A NP_079495.1:n.*2725G>A
XM_011529048.1:c.*2725G>A XP_011527350.1:n.*2725G>A
XM_011529049.1:c.*2725G>A XP_011527351.1:n.*2725G>A
XM_011529050.1:c.*2725G>A XP_011527352.1:n.*2725G>A
XR_936629.1:n.4028G>A
XR_936630.1:n.4286G>A
XM_011529048.2:c.*2725G>A XP_011527350.1:n.*2725G>A
XR_936629.2:n.4041G>A
NM_025219.3:c.*2725G>A MANE Select NP_079495.1:n.*2725G>A
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