Canonical Allele Identifier: CA479238543

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40340354C>T , CM000674.2:g.40340354C>T	GRCh38
NC_000012.11:g.40734156C>T , CM000674.1:g.40734156C>T	GRCh37
NC_000012.10:g.39020423C>T	NCBI36
NG_011709.1:g.120344C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_198578.4:c.6009C>T MANE Select	NP_940980.4:p.Phe2003=
ENST00000298910.12:c.6009C>T MANE Select	ENSP00000298910.7:p.Phe2003=
NM_198578.3:c.6009C>T	NP_940980.3:p.Phe2003=
ENST00000298910.11:c.6009C>T	ENSP00000298910.7:p.Phe2003=
ENST00000430804.5:c.3305C>T
ENST00000479187.5:n.2690C>T
ENST00000679360.1:c.*4918C>T	ENSP00000505368.1:n.*4918C>T
ENST00000679532.1:c.1783C>T
ENST00000680018.1:c.1454C>T	ENSP00000505347.1:n.1454C>T
ENST00000680422.1:c.1654C>T
ENST00000680425.1:c.1176C>T	ENSP00000506459.1:n.1176C>T
ENST00000680453.1:c.1466C>T
ENST00000680790.1:c.5754C>T	ENSP00000505335.1:p.Phe1918=
ENST00000681136.1:n.1993C>T
ENST00000681696.1:c.1692C>T	ENSP00000505871.1:p.Phe564=
XM_005268629.2:c.6009C>T	XP_005268686.1:p.Phe2003=
XM_005268629.4:c.6009C>T	XP_005268686.1:p.Phe2003=
XM_011537877.1:c.6009C>T	XP_011536179.1:p.Phe2003=
XM_011537877.3:c.6009C>T	XP_011536179.1:p.Phe2003=
XM_011537878.1:c.6009C>T	XP_011536180.1:p.Phe2003=
XM_011537879.1:c.4806C>T	XP_011536181.1:p.Phe1602=
XM_017018787.1:c.2925C>T	XP_016874276.1:p.Phe975=
XM_017018788.2:c.2271C>T	XP_016874277.1:p.Phe757=
XM_024448833.1:c.4806C>T	XP_024304601.1:p.Phe1602=