Canonical Allele Identifier: CA2031027113

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40340315T= , CM000674.2:g.40340315T=	GRCh38
NC_000012.11:g.40734117T= , CM000674.1:g.40734117T=	GRCh37
NC_000012.10:g.39020384T=	NCBI36
NG_011709.1:g.120305T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000298910.12:c.5970T= MANE Select	ENSP00000298910.7:p.Ile1990=
ENST00000679360.1:c.*4879T=	ENSP00000505368.1:n.*4879T=
ENST00000679532.1:c.1744T=
ENST00000680018.1:c.1415T=	ENSP00000505347.1:n.1415T=
ENST00000680422.1:c.1615T=
ENST00000680425.1:c.1137T=	ENSP00000506459.1:n.1137T=
ENST00000680453.1:c.1427T=
ENST00000680790.1:c.5715T=	ENSP00000505335.1:p.Ile1905=
ENST00000681136.1:n.1954T=
ENST00000681696.1:c.1653T=	ENSP00000505871.1:p.Ile551=
ENST00000298910.11:c.5970T=	ENSP00000298910.7:p.Ile1990=
ENST00000430804.5:c.3266T=
ENST00000479187.5:n.2651T=
NM_198578.3:c.5970T=	NP_940980.3:p.Ile1990=
XM_005268629.2:c.5970T=	XP_005268686.1:p.Ile1990=
XM_011537877.1:c.5970T=	XP_011536179.1:p.Ile1990=
XM_011537878.1:c.5970T=	XP_011536180.1:p.Ile1990=
XM_011537879.1:c.4767T=	XP_011536181.1:p.Ile1589=
XM_005268629.4:c.5970T=	XP_005268686.1:p.Ile1990=
XM_011537877.3:c.5970T=	XP_011536179.1:p.Ile1990=
XM_017018787.1:c.2886T=	XP_016874276.1:p.Ile962=
XM_017018788.2:c.2232T=	XP_016874277.1:p.Ile744=
XM_024448833.1:c.4767T=	XP_024304601.1:p.Ile1589=
NM_198578.4:c.5970T= MANE Select	NP_940980.4:p.Ile1990=