Canonical Allele Identifier: CA479247528

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40757315T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40363513T>A , CM000674.2:g.40363513T>A	GRCh38
NC_000012.11:g.40757315T>A , CM000674.1:g.40757315T>A	GRCh37
NC_000012.10:g.39043582T>A	NCBI36
NG_011709.1:g.143503T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.7140T>A MANE Select	ENSP00000298910.7:p.Thr2380=
ENST00000636518.1:c.937T>A
ENST00000679360.1:c.*6049T>A	ENSP00000505368.1:n.*6049T>A
ENST00000679532.1:c.2914T>A
ENST00000679683.1:c.930T>A
ENST00000680018.1:c.2585T>A	ENSP00000505347.1:n.2585T>A
ENST00000680422.1:c.4227T>A
ENST00000680425.1:c.2307T>A	ENSP00000506459.1:n.2307T>A
ENST00000680453.1:c.2597T>A
ENST00000680790.1:c.6885T>A	ENSP00000505335.1:p.Thr2295=
ENST00000681136.1:n.3124T>A
ENST00000681696.1:c.2823T>A	ENSP00000505871.1:p.Thr941=
ENST00000681773.1:n.347T>A
ENST00000298910.11:c.7140T>A	ENSP00000298910.7:p.Thr2380=
ENST00000430804.5:c.4436T>A
ENST00000479187.5:n.3821T>A
NM_198578.3:c.7140T>A	NP_940980.3:p.Thr2380=
XM_005268629.2:c.7140T>A	XP_005268686.1:p.Thr2380=
XM_011537877.1:c.7140T>A	XP_011536179.1:p.Thr2380=
XM_011537879.1:c.5937T>A	XP_011536181.1:p.Thr1979=
XR_944868.1:n.485-8686A>T
XM_005268629.4:c.7140T>A	XP_005268686.1:p.Thr2380=
XM_011537877.3:c.7140T>A	XP_011536179.1:p.Thr2380=
XM_017018787.1:c.4056T>A	XP_016874276.1:p.Thr1352=
XM_017018788.2:c.3402T>A	XP_016874277.1:p.Thr1134=
XM_024448833.1:c.5937T>A	XP_024304601.1:p.Thr1979=
XR_944868.2:n.485-8686A>T
NM_198578.4:c.7140T>A MANE Select	NP_940980.4:p.Thr2380=