Canonical Allele Identifier: CA384406884

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40745431A>T (hg19) ; chr12:g.40351629A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40351629A>T , CM000674.2:g.40351629A>T	GRCh38
NC_000012.11:g.40745431A>T , CM000674.1:g.40745431A>T	GRCh37
NC_000012.10:g.39031698A>T	NCBI36
NG_011709.1:g.131619A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.6472A>T MANE Select	ENSP00000298910.7:p.Thr2158Ser
ENST00000636518.1:c.269A>T
ENST00000679360.1:c.*5381A>T	ENSP00000505368.1:n.*5381A>T
ENST00000679532.1:c.2246A>T
ENST00000679683.1:c.262A>T
ENST00000680018.1:c.1917A>T	ENSP00000505347.1:n.1917A>T
ENST00000680422.1:c.2117A>T
ENST00000680425.1:c.1639A>T	ENSP00000506459.1:n.1639A>T
ENST00000680453.1:c.1929A>T
ENST00000680790.1:c.6217A>T	ENSP00000505335.1:p.Thr2073Ser
ENST00000681136.1:n.2456A>T
ENST00000681696.1:c.2155A>T	ENSP00000505871.1:p.Thr719Ser
ENST00000298910.11:c.6472A>T	ENSP00000298910.7:p.Thr2158Ser
ENST00000430804.5:c.3768A>T
ENST00000479187.5:n.3153A>T
NM_198578.3:c.6472A>T	NP_940980.3:p.Thr2158Ser
XM_005268629.2:c.6472A>T	XP_005268686.1:p.Thr2158Ser
XM_011537877.1:c.6472A>T	XP_011536179.1:p.Thr2158Ser
XM_011537878.1:c.6472A>T	XP_011536180.1:p.Thr2158Ser
XM_011537879.1:c.5269A>T	XP_011536181.1:p.Thr1757Ser
XM_005268629.4:c.6472A>T	XP_005268686.1:p.Thr2158Ser
XM_011537877.3:c.6472A>T	XP_011536179.1:p.Thr2158Ser
XM_017018787.1:c.3388A>T	XP_016874276.1:p.Thr1130Ser
XM_017018788.2:c.2734A>T	XP_016874277.1:p.Thr912Ser
XM_024448833.1:c.5269A>T	XP_024304601.1:p.Thr1757Ser
NM_198578.4:c.6472A>T MANE Select	NP_940980.4:p.Thr2158Ser