Canonical Allele Identifier: CA479241359

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40745427T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40351625T>A , CM000674.2:g.40351625T>A	GRCh38
NC_000012.11:g.40745427T>A , CM000674.1:g.40745427T>A	GRCh37
NC_000012.10:g.39031694T>A	NCBI36
NG_011709.1:g.131615T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.6468T>A MANE Select	ENSP00000298910.7:p.Val2156=
ENST00000636518.1:c.265T>A
ENST00000679360.1:c.*5377T>A	ENSP00000505368.1:n.*5377T>A
ENST00000679532.1:c.2242T>A
ENST00000679683.1:c.258T>A
ENST00000680018.1:c.1913T>A	ENSP00000505347.1:n.1913T>A
ENST00000680422.1:c.2113T>A
ENST00000680425.1:c.1635T>A	ENSP00000506459.1:n.1635T>A
ENST00000680453.1:c.1925T>A
ENST00000680790.1:c.6213T>A	ENSP00000505335.1:p.Val2071=
ENST00000681136.1:n.2452T>A
ENST00000681696.1:c.2151T>A	ENSP00000505871.1:p.Val717=
ENST00000298910.11:c.6468T>A	ENSP00000298910.7:p.Val2156=
ENST00000430804.5:c.3764T>A
ENST00000479187.5:n.3149T>A
NM_198578.3:c.6468T>A	NP_940980.3:p.Val2156=
XM_005268629.2:c.6468T>A	XP_005268686.1:p.Val2156=
XM_011537877.1:c.6468T>A	XP_011536179.1:p.Val2156=
XM_011537878.1:c.6468T>A	XP_011536180.1:p.Val2156=
XM_011537879.1:c.5265T>A	XP_011536181.1:p.Val1755=
XM_005268629.4:c.6468T>A	XP_005268686.1:p.Val2156=
XM_011537877.3:c.6468T>A	XP_011536179.1:p.Val2156=
XM_017018787.1:c.3384T>A	XP_016874276.1:p.Val1128=
XM_017018788.2:c.2730T>A	XP_016874277.1:p.Val910=
XM_024448833.1:c.5265T>A	XP_024304601.1:p.Val1755=
NM_198578.4:c.6468T>A MANE Select	NP_940980.4:p.Val2156=