Canonical Allele Identifier: CA384413225

Gene: LRRK2

Linked Data

• dbSNP Id: rs1946777602
• gnomAD v3: 12-40363437-T-C
• gnomAD v4: 12-40363437-T-C
• MyVariant Identifiers: chr12:g.40757239T>C (hg19) ; chr12:g.40363437T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40363437T>C , CM000674.2:g.40363437T>C	GRCh38
NC_000012.11:g.40757239T>C , CM000674.1:g.40757239T>C	GRCh37
NC_000012.10:g.39043506T>C	NCBI36
NG_011709.1:g.143427T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000298910.12:c.7064T>C MANE Select	ENSP00000298910.7:p.Ile2355Thr
ENST00000636518.1:c.861T>C
ENST00000679360.1:c.*5973T>C	ENSP00000505368.1:n.*5973T>C
ENST00000679532.1:c.2838T>C
ENST00000679683.1:c.854T>C
ENST00000680018.1:c.2509T>C	ENSP00000505347.1:n.2509T>C
ENST00000680422.1:c.4151T>C
ENST00000680425.1:c.2231T>C	ENSP00000506459.1:n.2231T>C
ENST00000680453.1:c.2521T>C
ENST00000680790.1:c.6809T>C	ENSP00000505335.1:p.Ile2270Thr
ENST00000681136.1:n.3048T>C
ENST00000681696.1:c.2747T>C	ENSP00000505871.1:p.Ile916Thr
ENST00000681773.1:n.271T>C
ENST00000298910.11:c.7064T>C	ENSP00000298910.7:p.Ile2355Thr
ENST00000430804.5:c.4360T>C
ENST00000479187.5:n.3745T>C
NM_198578.3:c.7064T>C	NP_940980.3:p.Ile2355Thr
XM_005268629.2:c.7064T>C	XP_005268686.1:p.Ile2355Thr
XM_011537877.1:c.7064T>C	XP_011536179.1:p.Ile2355Thr
XM_011537879.1:c.5861T>C	XP_011536181.1:p.Ile1954Thr
XR_944868.1:n.485-8610A>G
XM_005268629.4:c.7064T>C	XP_005268686.1:p.Ile2355Thr
XM_011537877.3:c.7064T>C	XP_011536179.1:p.Ile2355Thr
XM_017018787.1:c.3980T>C	XP_016874276.1:p.Ile1327Thr
XM_017018788.2:c.3326T>C	XP_016874277.1:p.Ile1109Thr
XM_024448833.1:c.5861T>C	XP_024304601.1:p.Ile1954Thr
XR_944868.2:n.485-8610A>G
NM_198578.4:c.7064T>C MANE Select	NP_940980.4:p.Ile2355Thr