Canonical Allele Identifier: CA384404091

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40734227T>G (hg19) ; chr12:g.40340425T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40340425T>G , CM000674.2:g.40340425T>G	GRCh38
NC_000012.11:g.40734227T>G , CM000674.1:g.40734227T>G	GRCh37
NC_000012.10:g.39020494T>G	NCBI36
NG_011709.1:g.120415T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000298910.12:c.6080T>G MANE Select	ENSP00000298910.7:p.Met2027Arg
ENST00000679360.1:c.*4989T>G	ENSP00000505368.1:n.*4989T>G
ENST00000679532.1:c.1854T>G
ENST00000680018.1:c.1525T>G	ENSP00000505347.1:n.1525T>G
ENST00000680422.1:c.1725T>G
ENST00000680425.1:c.1247T>G	ENSP00000506459.1:n.1247T>G
ENST00000680453.1:c.1537T>G
ENST00000680790.1:c.5825T>G	ENSP00000505335.1:p.Met1942Arg
ENST00000681136.1:n.2064T>G
ENST00000681696.1:c.1763T>G	ENSP00000505871.1:p.Met588Arg
ENST00000298910.11:c.6080T>G	ENSP00000298910.7:p.Met2027Arg
ENST00000430804.5:c.3376T>G
ENST00000479187.5:n.2761T>G
NM_198578.3:c.6080T>G	NP_940980.3:p.Met2027Arg
XM_005268629.2:c.6080T>G	XP_005268686.1:p.Met2027Arg
XM_011537877.1:c.6080T>G	XP_011536179.1:p.Met2027Arg
XM_011537878.1:c.6080T>G	XP_011536180.1:p.Met2027Arg
XM_011537879.1:c.4877T>G	XP_011536181.1:p.Met1626Arg
XM_005268629.4:c.6080T>G	XP_005268686.1:p.Met2027Arg
XM_011537877.3:c.6080T>G	XP_011536179.1:p.Met2027Arg
XM_017018787.1:c.2996T>G	XP_016874276.1:p.Met999Arg
XM_017018788.2:c.2342T>G	XP_016874277.1:p.Met781Arg
XM_024448833.1:c.4877T>G	XP_024304601.1:p.Met1626Arg
NM_198578.4:c.6080T>G MANE Select	NP_940980.4:p.Met2027Arg