Canonical Allele Identifier: CA16620983
Gene: DNAJC5 HGNC NCBI

Linked Data

ClinVar Variation Id: 418748
ClinVar RCV Id: RCV000487294
dbSNP Id: rs1345043761
gnomAD v2: 20-62526627-A-AGCGGAGCC
gnomAD v3: 20-63895274-A-AGCGGAGCC
gnomAD v4: 20-63895274-A-AGCGGAGCC
MyVariant Identifiers: chr20:g.62526637_62526644dupCGGAGCCG (hg19) chr20:g.62526635_62526636insGCGGAGCC (hg19) chr20:g.62526627_62526628insGCGGAGCC (hg19) chr20:g.63895284_63895291dupCGGAGCCG (hg38) chr20:g.63895282_63895283insGCGGAGCC (hg38) chr20:g.63895274_63895275insGCGGAGCC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63895284_63895291dup , CM000682.2:g.63895284_63895291dup GRCh38
NC_000020.10:g.62526637_62526644dup , CM000682.1:g.62526637_62526644dup GRCh37
NC_000020.9:g.61997081_61997088dup NCBI36
NG_029805.1:g.5183_5190dup
NG_029805.2:g.5183_5190dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000360864.9:c.-51_-44dup MANE Select ENSP00000354111.4:n.-51_-44dup
ENST00000360864.8:c.-51_-44dup ENSP00000354111.4:n.-51_-44dup
ENST00000470551.1:c.-51_-44dup ENSP00000434744.1:n.-51_-44dup
NM_025219.2:c.-51_-44dup NP_079495.1:n.-51_-44dup
NM_025219.3:c.-51_-44dup MANE Select NP_079495.1:n.-51_-44dup
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