Canonical Allele Identifier: CA2697549750

Gene: DNAJB6

Linked Data

• ClinVar Variation Id: 2694853
• ClinVar RCV Id: RCV003525462

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.157367502T>A , CM000669.2:g.157367502T>A	GRCh38
NC_000007.13:g.157160196T>A , CM000669.1:g.157160196T>A	GRCh37
NC_000007.12:g.156852957T>A	NCBI36
NG_032573.1:g.35487T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262177.9:c.346+19T>A MANE Select	ENSP00000262177.4:n.346+19T>A
ENST00000262177.8:c.346+19T>A	ENSP00000262177.4:n.346+19T>A
ENST00000412557.5:c.346+19T>A	ENSP00000403407.1:n.346+19T>A
ENST00000417758.5:c.346+19T>A	ENSP00000400665.1:n.346+19T>A
ENST00000429029.6:c.346+19T>A	ENSP00000397556.2:n.346+19T>A
ENST00000441291.5:c.346+19T>A	ENSP00000415201.1:n.346+19T>A
ENST00000441561.5:c.346+19T>A	ENSP00000410643.1:n.346+19T>A
ENST00000443280.5:c.346+19T>A	ENSP00000396267.1:n.346+19T>A
ENST00000459889.5:c.346+19T>A	ENSP00000488263.1:n.346+19T>A
ENST00000486083.6:n.513+19T>A
ENST00000488001.5:n.492+19T>A
ENST00000634080.1:c.346+19T>A	ENSP00000488740.1:n.346+19T>A
NM_005494.2:c.346+19T>A	NP_005485.1:n.346+19T>A
NM_058246.3:c.346+19T>A	NP_490647.1:n.346+19T>A
XM_005249515.2:c.346+19T>A	XP_005249572.1:n.346+19T>A
XM_005249516.2:c.346+19T>A	XP_005249573.1:n.346+19T>A
XM_006715823.1:c.346+19T>A	XP_006715886.1:n.346+19T>A
XM_011515704.1:c.346+19T>A	XP_011514006.1:n.346+19T>A
NM_001363676.1:c.346+19T>A	NP_001350605.1:n.346+19T>A
XM_005249515.3:c.346+19T>A	XP_005249572.1:n.346+19T>A
XM_006715823.2:c.346+19T>A	XP_006715886.1:n.346+19T>A
NM_058246.4:c.346+19T>A MANE Select	NP_490647.1:n.346+19T>A
NM_005494.3:c.346+19T>A	NP_005485.1:n.346+19T>A