Canonical Allele Identifier: CA384413547

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40757327T>G (hg19) ; chr12:g.40363525T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40363525T>G , CM000674.2:g.40363525T>G	GRCh38
NC_000012.11:g.40757327T>G , CM000674.1:g.40757327T>G	GRCh37
NC_000012.10:g.39043594T>G	NCBI36
NG_011709.1:g.143515T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.7152T>G MANE Select	ENSP00000298910.7:p.Cys2384Trp
ENST00000636518.1:c.949T>G
ENST00000679360.1:c.*6061T>G	ENSP00000505368.1:n.*6061T>G
ENST00000679532.1:c.2926T>G
ENST00000679683.1:c.942T>G
ENST00000680018.1:c.2597T>G	ENSP00000505347.1:n.2597T>G
ENST00000680422.1:c.4239T>G
ENST00000680425.1:c.2319T>G	ENSP00000506459.1:n.2319T>G
ENST00000680453.1:c.2609T>G
ENST00000680790.1:c.6897T>G	ENSP00000505335.1:p.Cys2299Trp
ENST00000681136.1:n.3136T>G
ENST00000681696.1:c.2835T>G	ENSP00000505871.1:p.Cys945Trp
ENST00000681773.1:n.359T>G
ENST00000298910.11:c.7152T>G	ENSP00000298910.7:p.Cys2384Trp
ENST00000430804.5:c.4448T>G
ENST00000479187.5:n.3833T>G
NM_198578.3:c.7152T>G	NP_940980.3:p.Cys2384Trp
XM_005268629.2:c.7152T>G	XP_005268686.1:p.Cys2384Trp
XM_011537877.1:c.7152T>G	XP_011536179.1:p.Cys2384Trp
XM_011537879.1:c.5949T>G	XP_011536181.1:p.Cys1983Trp
XR_944868.1:n.485-8698A>C
XM_005268629.4:c.7152T>G	XP_005268686.1:p.Cys2384Trp
XM_011537877.3:c.7152T>G	XP_011536179.1:p.Cys2384Trp
XM_017018787.1:c.4068T>G	XP_016874276.1:p.Cys1356Trp
XM_017018788.2:c.3414T>G	XP_016874277.1:p.Cys1138Trp
XM_024448833.1:c.5949T>G	XP_024304601.1:p.Cys1983Trp
XR_944868.2:n.485-8698A>C
NM_198578.4:c.7152T>G MANE Select	NP_940980.4:p.Cys2384Trp