Canonical Allele Identifier: CA373272821

Gene: DNAJB5

Linked Data

• ClinVar Variation Id: 1695248
• ClinVar RCV Id: RCV002263498
• dbSNP Id: rs1384468289
• MyVariant Identifiers: chr9:g.34996282A>T (hg19) ; chr9:g.34996285A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34996285A>T , CM000671.2:g.34996285A>T	GRCh38
NC_000009.11:g.34996282A>T , CM000671.1:g.34996282A>T	GRCh37
NC_000009.10:g.34986282A>T	NCBI36
NG_053054.1:g.11917A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682809.1:c.448A>T MANE Select	ENSP00000507741.1:p.Thr150Ser
ENST00000684748.1:c.232A>T	ENSP00000506753.1:p.Thr78Ser
ENST00000453597.8:c.334A>T	ENSP00000404079.4:p.Thr112Ser
ENST00000312316.9:c.232A>T	ENSP00000312517.5:p.Thr78Ser
ENST00000443266.2:c.232A>T	ENSP00000396332.1:p.Thr78Ser
ENST00000453597.7:c.574A>T	ENSP00000404079.3:p.Thr192Ser
ENST00000454002.6:c.448A>T	ENSP00000413684.2:p.Thr150Ser
ENST00000469798.5:c.212-110A>T	ENSP00000433640.2:n.212-110A>T
ENST00000537321.5:c.232A>T	ENSP00000439217.2:p.Thr78Ser
ENST00000539059.1:c.292A>T	ENSP00000445536.2:p.Thr98Ser
ENST00000541010.5:n.3244A>T
ENST00000545841.5:c.232A>T	ENSP00000441999.1:p.Thr78Ser
NM_001135004.2:c.574A>T	NP_001128476.2:p.Thr192Ser
NM_001135005.2:c.448A>T	NP_001128477.1:p.Thr150Ser
NM_012266.5:c.232A>T	NP_036398.3:p.Thr78Ser
XM_005251428.3:c.232A>T	XP_005251485.1:p.Thr78Ser
XM_006716751.2:c.232A>T	XP_006716814.1:p.Thr78Ser
XM_011517842.1:c.448A>T	XP_011516144.1:p.Thr150Ser
NM_001349723.1:c.448A>T	NP_001336652.1:p.Thr150Ser
NM_001349724.1:c.232A>T	NP_001336653.1:p.Thr78Ser
NM_001349725.1:c.571A>T	NP_001336654.1:p.Thr191Ser
NM_001135004.3:c.334A>T	NP_001128476.3:p.Thr112Ser
NM_001135005.3:c.448A>T	NP_001128477.1:p.Thr150Ser
NM_001349723.2:c.448A>T	NP_001336652.1:p.Thr150Ser
NM_001349724.2:c.232A>T	NP_001336653.1:p.Thr78Ser
NM_001349725.2:c.334A>T	NP_001336654.2:p.Thr112Ser
NM_012266.6:c.232A>T	NP_036398.3:p.Thr78Ser
NM_001349723.3:c.448A>T MANE Select	NP_001336652.1:p.Thr150Ser