Canonical Allele Identifier: CA2031000143

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40351579C= , CM000674.2:g.40351579C=	GRCh38
NC_000012.11:g.40745381C= , CM000674.1:g.40745381C=	GRCh37
NC_000012.10:g.39031648C=	NCBI36
NG_011709.1:g.131569C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.6422C= MANE Select	ENSP00000298910.7:p.Thr2141=
ENST00000636518.1:c.219C=
ENST00000679360.1:c.*5331C=	ENSP00000505368.1:n.*5331C=
ENST00000679532.1:c.2196C=
ENST00000679683.1:c.212C=
ENST00000680018.1:c.1867C=	ENSP00000505347.1:n.1867C=
ENST00000680422.1:c.2067C=
ENST00000680425.1:c.1589C=	ENSP00000506459.1:n.1589C=
ENST00000680453.1:c.1879C=
ENST00000680790.1:c.6167C=	ENSP00000505335.1:p.Thr2056=
ENST00000681136.1:n.2406C=
ENST00000681696.1:c.2105C=	ENSP00000505871.1:p.Thr702=
ENST00000298910.11:c.6422C=	ENSP00000298910.7:p.Thr2141=
ENST00000430804.5:c.3718C=
ENST00000479187.5:n.3103C=
NM_198578.3:c.6422C=	NP_940980.3:p.Thr2141=
XM_005268629.2:c.6422C=	XP_005268686.1:p.Thr2141=
XM_011537877.1:c.6422C=	XP_011536179.1:p.Thr2141=
XM_011537878.1:c.6422C=	XP_011536180.1:p.Thr2141=
XM_011537879.1:c.5219C=	XP_011536181.1:p.Thr1740=
XM_005268629.4:c.6422C=	XP_005268686.1:p.Thr2141=
XM_011537877.3:c.6422C=	XP_011536179.1:p.Thr2141=
XM_017018787.1:c.3338C=	XP_016874276.1:p.Thr1113=
XM_017018788.2:c.2684C=	XP_016874277.1:p.Thr895=
XM_024448833.1:c.5219C=	XP_024304601.1:p.Thr1740=
NM_198578.4:c.6422C= MANE Select	NP_940980.4:p.Thr2141=