Canonical Allele Identifier: CA3100471156

Gene: DNAJB11

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186581393C= , CM000665.2:g.186581393C=	GRCh38
NC_000003.11:g.186299182C= , CM000665.1:g.186299182C=	GRCh37
NC_000003.10:g.187781876C=	NCBI36
NG_034024.1:g.15718C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265028.8:c.479C= MANE Select	ENSP00000265028.3:p.Ala160=
ENST00000464877.2:n.4247C=
ENST00000495390.2:n.4247C=
ENST00000679794.1:n.206C=
ENST00000680338.1:c.*210C=	ENSP00000505624.1:n.*210C=
ENST00000681475.1:n.91C=
ENST00000681543.1:n.1222C=
ENST00000265028.7:c.479C=	ENSP00000265028.3:p.Ala160=
ENST00000439351.5:c.479C=	ENSP00000414398.1:p.Ala160=
ENST00000495390.1:n.3096C=
NM_016306.5:c.479C=	NP_057390.1:p.Ala160=
NM_001378451.1:c.324-602C=	NP_001365380.1:n.324-602C=
NM_016306.6:c.479C= MANE Select	NP_057390.1:p.Ala160=
NR_165638.1:n.653C=
NR_165639.1:n.657C=
NR_165640.1:n.740C=
NR_165641.1:n.625C=
NR_165642.1:n.635-602C=
NR_165643.1:n.607C=