Canonical Allele Identifier: CA10606310

Gene: DNAJB6

Linked Data

• ClinVar Variation Id: 289051
• ClinVar RCV Id: RCV000300891 ; RCV001437753
• dbSNP Id: rs886044069
• MyVariant Identifiers: chr7:g.157177595C>A (hg19) ; chr7:g.157384901C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.157384901C>A , CM000669.2:g.157384901C>A	GRCh38
NC_000007.13:g.157177595C>A , CM000669.1:g.157177595C>A	GRCh37
NC_000007.12:g.156870356C>A	NCBI36
NG_032573.1:g.52886C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262177.9:c.513C>A MANE Select	ENSP00000262177.4:p.Gly171=
ENST00000262177.8:c.513C>A	ENSP00000262177.4:p.Gly171=
ENST00000417758.5:c.513C>A	ENSP00000400665.1:p.Gly171=
ENST00000429029.6:c.513C>A	ENSP00000397556.2:p.Gly171=
ENST00000443280.5:c.346+17418C>A	ENSP00000396267.1:n.346+17418C>A
ENST00000459889.5:c.513C>A	ENSP00000488263.1:p.Gly171=
ENST00000465908.5:n.309C>A
ENST00000468928.5:n.818C>A
ENST00000487480.1:n.4288C>A
ENST00000634080.1:c.513C>A	ENSP00000488740.1:p.Gly171=
NM_005494.2:c.513C>A	NP_005485.1:p.Gly171=
NM_058246.3:c.513C>A	NP_490647.1:p.Gly171=
XM_005249515.2:c.513C>A	XP_005249572.1:p.Gly171=
XM_005249516.2:c.513C>A	XP_005249573.1:p.Gly171=
XM_006715823.1:c.513C>A	XP_006715886.1:p.Gly171=
XM_011515704.1:c.513C>A	XP_011514006.1:p.Gly171=
NM_001363676.1:c.346+17418C>A	NP_001350605.1:n.346+17418C>A
XM_005249515.3:c.513C>A	XP_005249572.1:p.Gly171=
XM_006715823.2:c.513C>A	XP_006715886.1:p.Gly171=
NM_058246.4:c.513C>A MANE Select	NP_490647.1:p.Gly171=
NM_005494.3:c.513C>A	NP_005485.1:p.Gly171=