Canonical Allele Identifier: CA4590362
Gene: DNAJB6 HGNC NCBI

Linked Data

ClinVar Variation Id: 500303
dbSNP Id: rs575604496

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.157363244C>T , CM000669.2:g.157363244C>T GRCh38
NC_000007.13:g.157155938C>T , CM000669.1:g.157155938C>T GRCh37
NC_000007.12:g.156848699C>T NCBI36
NG_032573.1:g.31229C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262177.9:c.149C>T MANE Select ENSP00000262177.4:p.Ala50Val
ENST00000262177.8:c.149C>T ENSP00000262177.4:p.Ala50Val
ENST00000412557.5:c.149C>T ENSP00000403407.1:p.Ala50Val
ENST00000417758.5:c.149C>T ENSP00000400665.1:p.Ala50Val
ENST00000429029.6:c.149C>T ENSP00000397556.2:p.Ala50Val
ENST00000437030.5:c.149C>T ENSP00000391690.1:p.Ala50Val
ENST00000441291.5:c.149C>T ENSP00000415201.1:p.Ala50Val
ENST00000441561.5:c.149C>T ENSP00000410643.1:p.Ala50Val
ENST00000443280.5:c.149C>T ENSP00000396267.1:p.Ala50Val
ENST00000453383.5:c.149C>T ENSP00000396240.1:p.Ala50Val
ENST00000459889.5:c.149C>T ENSP00000488263.1:p.Ala50Val
ENST00000486083.6:n.316C>T
ENST00000488001.5:n.295C>T
ENST00000634080.1:c.149C>T ENSP00000488740.1:p.Ala50Val
NM_005494.2:c.149C>T NP_005485.1:p.Ala50Val
NM_058246.3:c.149C>T NP_490647.1:p.Ala50Val
XM_005249515.2:c.149C>T XP_005249572.1:p.Ala50Val
XM_005249516.2:c.149C>T XP_005249573.1:p.Ala50Val
XM_006715823.1:c.149C>T XP_006715886.1:p.Ala50Val
XM_011515704.1:c.149C>T XP_011514006.1:p.Ala50Val
NM_001363676.1:c.149C>T NP_001350605.1:p.Ala50Val
XM_005249515.3:c.149C>T XP_005249572.1:p.Ala50Val
XM_006715823.2:c.149C>T XP_006715886.1:p.Ala50Val
NM_058246.4:c.149C>T MANE Select NP_490647.1:p.Ala50Val
NM_005494.3:c.149C>T NP_005485.1:p.Ala50Val