Canonical Allele Identifier: CA384406486

Gene: LRRK2

Linked Data

• dbSNP Id: rs1325662029
• MyVariant Identifiers: chr12:g.40745354T>A (hg19) ; chr12:g.40351552T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40351552T>A , CM000674.2:g.40351552T>A	GRCh38
NC_000012.11:g.40745354T>A , CM000674.1:g.40745354T>A	GRCh37
NC_000012.10:g.39031621T>A	NCBI36
NG_011709.1:g.131542T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.6395T>A MANE Select	ENSP00000298910.7:p.Leu2132Ter
ENST00000636518.1:c.192T>A
ENST00000679360.1:c.*5304T>A	ENSP00000505368.1:n.*5304T>A
ENST00000679532.1:c.2169T>A
ENST00000679683.1:c.185T>A
ENST00000680018.1:c.1840T>A	ENSP00000505347.1:n.1840T>A
ENST00000680422.1:c.2040T>A
ENST00000680425.1:c.1562T>A	ENSP00000506459.1:n.1562T>A
ENST00000680453.1:c.1852T>A
ENST00000680790.1:c.6140T>A	ENSP00000505335.1:p.Leu2047Ter
ENST00000681136.1:n.2379T>A
ENST00000681696.1:c.2078T>A	ENSP00000505871.1:p.Leu693Ter
ENST00000298910.11:c.6395T>A	ENSP00000298910.7:p.Leu2132Ter
ENST00000430804.5:c.3691T>A
ENST00000479187.5:n.3076T>A
NM_198578.3:c.6395T>A	NP_940980.3:p.Leu2132Ter
XM_005268629.2:c.6395T>A	XP_005268686.1:p.Leu2132Ter
XM_011537877.1:c.6395T>A	XP_011536179.1:p.Leu2132Ter
XM_011537878.1:c.6395T>A	XP_011536180.1:p.Leu2132Ter
XM_011537879.1:c.5192T>A	XP_011536181.1:p.Leu1731Ter
XM_005268629.4:c.6395T>A	XP_005268686.1:p.Leu2132Ter
XM_011537877.3:c.6395T>A	XP_011536179.1:p.Leu2132Ter
XM_017018787.1:c.3311T>A	XP_016874276.1:p.Leu1104Ter
XM_017018788.2:c.2657T>A	XP_016874277.1:p.Leu886Ter
XM_024448833.1:c.5192T>A	XP_024304601.1:p.Leu1731Ter
NM_198578.4:c.6395T>A MANE Select	NP_940980.4:p.Leu2132Ter