Canonical Allele Identifier: CA1755530235

Gene: DNAJB6

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.157367478T= , CM000669.2:g.157367478T=	GRCh38
NC_000007.13:g.157160172T= , CM000669.1:g.157160172T=	GRCh37
NC_000007.12:g.156852933T=	NCBI36
NG_032573.1:g.35463T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262177.9:c.341T= MANE Select	ENSP00000262177.4:p.Phe114=
ENST00000262177.8:c.341T=	ENSP00000262177.4:p.Phe114=
ENST00000412557.5:c.341T=	ENSP00000403407.1:p.Phe114=
ENST00000417758.5:c.341T=	ENSP00000400665.1:p.Phe114=
ENST00000429029.6:c.341T=	ENSP00000397556.2:p.Phe114=
ENST00000441291.5:c.341T=	ENSP00000415201.1:p.Phe114=
ENST00000441561.5:c.341T=	ENSP00000410643.1:p.Phe114=
ENST00000443280.5:c.341T=	ENSP00000396267.1:p.Phe114=
ENST00000459889.5:c.341T=	ENSP00000488263.1:p.Phe114=
ENST00000486083.6:n.508T=
ENST00000488001.5:n.487T=
ENST00000634080.1:c.341T=	ENSP00000488740.1:p.Phe114=
NM_005494.2:c.341T=	NP_005485.1:p.Phe114=
NM_058246.3:c.341T=	NP_490647.1:p.Phe114=
XM_005249515.2:c.341T=	XP_005249572.1:p.Phe114=
XM_005249516.2:c.341T=	XP_005249573.1:p.Phe114=
XM_006715823.1:c.341T=	XP_006715886.1:p.Phe114=
XM_011515704.1:c.341T=	XP_011514006.1:p.Phe114=
NM_001363676.1:c.341T=	NP_001350605.1:p.Phe114=
XM_005249515.3:c.341T=	XP_005249572.1:p.Phe114=
XM_006715823.2:c.341T=	XP_006715886.1:p.Phe114=
NM_058246.4:c.341T= MANE Select	NP_490647.1:p.Phe114=
NM_005494.3:c.341T=	NP_005485.1:p.Phe114=