Canonical Allele Identifier: CA2031026062

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40363533T= , CM000674.2:g.40363533T=	GRCh38
NC_000012.11:g.40757335T= , CM000674.1:g.40757335T=	GRCh37
NC_000012.10:g.39043602T=	NCBI36
NG_011709.1:g.143523T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000298910.12:c.7160T= MANE Select	ENSP00000298910.7:p.Ile2387=
ENST00000636518.1:c.957T=
ENST00000679360.1:c.*6069T=	ENSP00000505368.1:n.*6069T=
ENST00000679532.1:c.2934T=
ENST00000679683.1:c.950T=
ENST00000680018.1:c.2605T=	ENSP00000505347.1:n.2605T=
ENST00000680422.1:c.4247T=
ENST00000680425.1:c.2327T=	ENSP00000506459.1:n.2327T=
ENST00000680453.1:c.2617T=
ENST00000680790.1:c.6905T=	ENSP00000505335.1:p.Ile2302=
ENST00000681136.1:n.3144T=
ENST00000681696.1:c.2843T=	ENSP00000505871.1:p.Ile948=
ENST00000681773.1:n.367T=
ENST00000298910.11:c.7160T=	ENSP00000298910.7:p.Ile2387=
ENST00000430804.5:c.4456T=
ENST00000479187.5:n.3841T=
NM_198578.3:c.7160T=	NP_940980.3:p.Ile2387=
XM_005268629.2:c.7160T=	XP_005268686.1:p.Ile2387=
XM_011537877.1:c.7160T=	XP_011536179.1:p.Ile2387=
XM_011537879.1:c.5957T=	XP_011536181.1:p.Ile1986=
XR_944868.1:n.485-8706A=
XM_005268629.4:c.7160T=	XP_005268686.1:p.Ile2387=
XM_011537877.3:c.7160T=	XP_011536179.1:p.Ile2387=
XM_017018787.1:c.4076T=	XP_016874276.1:p.Ile1359=
XM_017018788.2:c.3422T=	XP_016874277.1:p.Ile1141=
XM_024448833.1:c.5957T=	XP_024304601.1:p.Ile1986=
XR_944868.2:n.485-8706A=
NM_198578.4:c.7160T= MANE Select	NP_940980.4:p.Ile2387=