Canonical Allele Identifier: CA479241398

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40745433A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40351631A>G , CM000674.2:g.40351631A>G	GRCh38
NC_000012.11:g.40745433A>G , CM000674.1:g.40745433A>G	GRCh37
NC_000012.10:g.39031700A>G	NCBI36
NG_011709.1:g.131621A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.6474A>G MANE Select	ENSP00000298910.7:p.Thr2158=
ENST00000636518.1:c.271A>G
ENST00000679360.1:c.*5383A>G	ENSP00000505368.1:n.*5383A>G
ENST00000679532.1:c.2248A>G
ENST00000679683.1:c.264A>G
ENST00000680018.1:c.1919A>G	ENSP00000505347.1:n.1919A>G
ENST00000680422.1:c.2119A>G
ENST00000680425.1:c.1641A>G	ENSP00000506459.1:n.1641A>G
ENST00000680453.1:c.1931A>G
ENST00000680790.1:c.6219A>G	ENSP00000505335.1:p.Thr2073=
ENST00000681136.1:n.2458A>G
ENST00000681696.1:c.2157A>G	ENSP00000505871.1:p.Thr719=
ENST00000298910.11:c.6474A>G	ENSP00000298910.7:p.Thr2158=
ENST00000430804.5:c.3770A>G
ENST00000479187.5:n.3155A>G
NM_198578.3:c.6474A>G	NP_940980.3:p.Thr2158=
XM_005268629.2:c.6474A>G	XP_005268686.1:p.Thr2158=
XM_011537877.1:c.6474A>G	XP_011536179.1:p.Thr2158=
XM_011537878.1:c.6474A>G	XP_011536180.1:p.Thr2158=
XM_011537879.1:c.5271A>G	XP_011536181.1:p.Thr1757=
XM_005268629.4:c.6474A>G	XP_005268686.1:p.Thr2158=
XM_011537877.3:c.6474A>G	XP_011536179.1:p.Thr2158=
XM_017018787.1:c.3390A>G	XP_016874276.1:p.Thr1130=
XM_017018788.2:c.2736A>G	XP_016874277.1:p.Thr912=
XM_024448833.1:c.5271A>G	XP_024304601.1:p.Thr1757=
NM_198578.4:c.6474A>G MANE Select	NP_940980.4:p.Thr2158=