Canonical Allele Identifier: CA1426998205

Gene: DNAJB11

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186572187C= , CM000665.2:g.186572187C=	GRCh38
NC_000003.11:g.186289976C= , CM000665.1:g.186289976C=	GRCh37
NC_000003.10:g.187772670C=	NCBI36
NG_034024.1:g.6512C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265028.8:c.161C= MANE Select	ENSP00000265028.3:p.Pro54=
ENST00000464877.2:n.359C=
ENST00000495390.2:n.359C=
ENST00000680338.1:c.161C=	ENSP00000505624.1:p.Pro54=
ENST00000265028.7:c.161C=	ENSP00000265028.3:p.Pro54=
ENST00000439351.5:c.161C=	ENSP00000414398.1:p.Pro54=
ENST00000464877.1:n.84C=
NM_016306.5:c.161C=	NP_057390.1:p.Pro54=
NM_001378451.1:c.161C=	NP_001365380.1:p.Pro54=
NM_016306.6:c.161C= MANE Select	NP_057390.1:p.Pro54=
NR_165638.1:n.339C=
NR_165639.1:n.339C=
NR_165640.1:n.339C=
NR_165641.1:n.339C=
NR_165642.1:n.339C=
NR_165643.1:n.339C=