Canonical Allele Identifier: CA10604559

Gene: DNAJB6

Linked Data

• ClinVar Variation Id: 283684
• ClinVar RCV Id: RCV000396152 ; RCV001471744
• dbSNP Id: rs886042682
• gnomAD v4: 7-157358635-G-A
• MyVariant Identifiers: chr7:g.157151329G>A (hg19) ; chr7:g.157358635G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.157358635G>A , CM000669.2:g.157358635G>A	GRCh38
NC_000007.13:g.157151329G>A , CM000669.1:g.157151329G>A	GRCh37
NC_000007.12:g.156844090G>A	NCBI36
NG_032573.1:g.26620G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262177.9:c.63G>A MANE Select	ENSP00000262177.4:p.Lys21=
ENST00000262177.8:c.63G>A	ENSP00000262177.4:p.Lys21=
ENST00000412557.5:c.63G>A	ENSP00000403407.1:p.Lys21=
ENST00000417758.5:c.63G>A	ENSP00000400665.1:p.Lys21=
ENST00000429029.6:c.63G>A	ENSP00000397556.2:p.Lys21=
ENST00000437030.5:c.63G>A	ENSP00000391690.1:p.Lys21=
ENST00000439402.1:c.63G>A	ENSP00000389599.1:p.Lys21=
ENST00000441291.5:c.63G>A	ENSP00000415201.1:p.Lys21=
ENST00000441561.5:c.63G>A	ENSP00000410643.1:p.Lys21=
ENST00000443280.5:c.63G>A	ENSP00000396267.1:p.Lys21=
ENST00000453383.5:c.63G>A	ENSP00000396240.1:p.Lys21=
ENST00000459889.5:c.63G>A	ENSP00000488263.1:p.Lys21=
ENST00000486083.6:n.230G>A
ENST00000488001.5:n.209G>A
ENST00000634080.1:c.63G>A	ENSP00000488740.1:p.Lys21=
NM_005494.2:c.63G>A	NP_005485.1:p.Lys21=
NM_058246.3:c.63G>A	NP_490647.1:p.Lys21=
XM_005249515.2:c.63G>A	XP_005249572.1:p.Lys21=
XM_005249516.2:c.63G>A	XP_005249573.1:p.Lys21=
XM_006715823.1:c.63G>A	XP_006715886.1:p.Lys21=
XM_011515704.1:c.63G>A	XP_011514006.1:p.Lys21=
NM_001363676.1:c.63G>A	NP_001350605.1:p.Lys21=
XM_005249515.3:c.63G>A	XP_005249572.1:p.Lys21=
XM_006715823.2:c.63G>A	XP_006715886.1:p.Lys21=
NM_058246.4:c.63G>A MANE Select	NP_490647.1:p.Lys21=
NM_005494.3:c.63G>A	NP_005485.1:p.Lys21=