Canonical Allele Identifier: CA1329145139

Gene: DNAJB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219281995T= , CM000664.2:g.219281995T=	GRCh38
NC_000002.11:g.220146717T= , CM000664.1:g.220146717T=	GRCh37
NC_000002.10:g.219854961T=	NCBI36
NG_029553.1:g.7678T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683651.1:n.989T=
ENST00000684599.1:n.493T=
ENST00000336576.10:c.286T= MANE Select	ENSP00000338019.5:p.Phe96=
ENST00000336576.9:c.286T=	ENSP00000338019.5:p.Phe96=
ENST00000392086.8:c.286T=	ENSP00000375936.4:p.Phe96=
ENST00000392087.6:c.286T=	ENSP00000375937.2:p.Phe96=
ENST00000421532.5:c.286T=	ENSP00000395173.1:p.Phe96=
ENST00000425450.5:c.286T=	ENSP00000414796.1:p.Phe96=
ENST00000439026.1:c.286T=	ENSP00000387951.1:p.Phe96=
ENST00000442681.5:c.286T=	ENSP00000392790.1:p.Phe96=
ENST00000463463.5:n.277T=
ENST00000477917.5:n.1504T=
ENST00000480537.5:n.474T=
ENST00000487855.1:n.186T=
NM_001039550.1:c.286T=	NP_001034639.1:p.Phe96=
NM_006736.5:c.286T=	NP_006727.2:p.Phe96=
NM_001039550.2:c.286T=	NP_001034639.1:p.Phe96=
NM_006736.6:c.286T= MANE Select	NP_006727.2:p.Phe96=