Canonical Allele Identifier: CA1329145131

Gene: DNAJB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219281977C= , CM000664.2:g.219281977C=	GRCh38
NC_000002.11:g.220146699C= , CM000664.1:g.220146699C=	GRCh37
NC_000002.10:g.219854943C=	NCBI36
NG_029553.1:g.7660C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683651.1:n.971C=
ENST00000684599.1:n.475C=
ENST00000336576.10:c.268C= MANE Select	ENSP00000338019.5:p.Pro90=
ENST00000336576.9:c.268C=	ENSP00000338019.5:p.Pro90=
ENST00000392086.8:c.268C=	ENSP00000375936.4:p.Pro90=
ENST00000392087.6:c.268C=	ENSP00000375937.2:p.Pro90=
ENST00000421532.5:c.268C=	ENSP00000395173.1:p.Pro90=
ENST00000425450.5:c.268C=	ENSP00000414796.1:p.Pro90=
ENST00000439026.1:c.268C=	ENSP00000387951.1:p.Pro90=
ENST00000442681.5:c.268C=	ENSP00000392790.1:p.Pro90=
ENST00000463463.5:n.259C=
ENST00000477917.5:n.1486C=
ENST00000480537.5:n.456C=
ENST00000487855.1:n.168C=
NM_001039550.1:c.268C=	NP_001034639.1:p.Pro90=
NM_006736.5:c.268C=	NP_006727.2:p.Pro90=
NM_001039550.2:c.268C=	NP_001034639.1:p.Pro90=
NM_006736.6:c.268C= MANE Select	NP_006727.2:p.Pro90=