Canonical Allele Identifier: CA384404096

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40734228G>T (hg19) ; chr12:g.40340426G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40340426G>T , CM000674.2:g.40340426G>T	GRCh38
NC_000012.11:g.40734228G>T , CM000674.1:g.40734228G>T	GRCh37
NC_000012.10:g.39020495G>T	NCBI36
NG_011709.1:g.120416G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000298910.12:c.6081G>T MANE Select	ENSP00000298910.7:p.Met2027Ile
ENST00000679360.1:c.*4990G>T	ENSP00000505368.1:n.*4990G>T
ENST00000679532.1:c.1855G>T
ENST00000680018.1:c.1526G>T	ENSP00000505347.1:n.1526G>T
ENST00000680422.1:c.1726G>T
ENST00000680425.1:c.1248G>T	ENSP00000506459.1:n.1248G>T
ENST00000680453.1:c.1538G>T
ENST00000680790.1:c.5826G>T	ENSP00000505335.1:p.Met1942Ile
ENST00000681136.1:n.2065G>T
ENST00000681696.1:c.1764G>T	ENSP00000505871.1:p.Met588Ile
ENST00000298910.11:c.6081G>T	ENSP00000298910.7:p.Met2027Ile
ENST00000430804.5:c.3377G>T
ENST00000479187.5:n.2762G>T
NM_198578.3:c.6081G>T	NP_940980.3:p.Met2027Ile
XM_005268629.2:c.6081G>T	XP_005268686.1:p.Met2027Ile
XM_011537877.1:c.6081G>T	XP_011536179.1:p.Met2027Ile
XM_011537878.1:c.6081G>T	XP_011536180.1:p.Met2027Ile
XM_011537879.1:c.4878G>T	XP_011536181.1:p.Met1626Ile
XM_005268629.4:c.6081G>T	XP_005268686.1:p.Met2027Ile
XM_011537877.3:c.6081G>T	XP_011536179.1:p.Met2027Ile
XM_017018787.1:c.2997G>T	XP_016874276.1:p.Met999Ile
XM_017018788.2:c.2343G>T	XP_016874277.1:p.Met781Ile
XM_024448833.1:c.4878G>T	XP_024304601.1:p.Met1626Ile
NM_198578.4:c.6081G>T MANE Select	NP_940980.4:p.Met2027Ile