Canonical Allele Identifier: CA10650193
Gene: DNAJC5 HGNC NCBI

Linked Data

ClinVar Variation Id: 339353
dbSNP Id: rs886056932

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63895240G>C , CM000682.2:g.63895240G>C GRCh38
NC_000020.10:g.62526593G>C , CM000682.1:g.62526593G>C GRCh37
NC_000020.9:g.61997037G>C NCBI36
NG_029805.1:g.5139G>C
NG_029805.2:g.5139G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360864.9:c.-95G>C MANE Select ENSP00000354111.4:n.-95G>C
ENST00000360864.8:c.-95G>C ENSP00000354111.4:n.-95G>C
ENST00000470551.1:c.-95G>C ENSP00000434744.1:n.-95G>C
NM_025219.2:c.-95G>C NP_079495.1:n.-95G>C
NM_025219.3:c.-95G>C MANE Select NP_079495.1:n.-95G>C