Canonical Allele Identifier: CA384404147

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40734239C>G (hg19) ; chr12:g.40340437C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40340437C>G , CM000674.2:g.40340437C>G	GRCh38
NC_000012.11:g.40734239C>G , CM000674.1:g.40734239C>G	GRCh37
NC_000012.10:g.39020506C>G	NCBI36
NG_011709.1:g.120427C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000298910.12:c.6092C>G MANE Select	ENSP00000298910.7:p.Thr2031Arg
ENST00000679360.1:c.*5001C>G	ENSP00000505368.1:n.*5001C>G
ENST00000679532.1:c.1866C>G
ENST00000680018.1:c.1537C>G	ENSP00000505347.1:n.1537C>G
ENST00000680422.1:c.1737C>G
ENST00000680425.1:c.1259C>G	ENSP00000506459.1:n.1259C>G
ENST00000680453.1:c.1549C>G
ENST00000680790.1:c.5837C>G	ENSP00000505335.1:p.Thr1946Arg
ENST00000681136.1:n.2076C>G
ENST00000681696.1:c.1775C>G	ENSP00000505871.1:p.Thr592Arg
ENST00000298910.11:c.6092C>G	ENSP00000298910.7:p.Thr2031Arg
ENST00000430804.5:c.3388C>G
ENST00000479187.5:n.2773C>G
NM_198578.3:c.6092C>G	NP_940980.3:p.Thr2031Arg
XM_005268629.2:c.6092C>G	XP_005268686.1:p.Thr2031Arg
XM_011537877.1:c.6092C>G	XP_011536179.1:p.Thr2031Arg
XM_011537878.1:c.6092C>G	XP_011536180.1:p.Thr2031Arg
XM_011537879.1:c.4889C>G	XP_011536181.1:p.Thr1630Arg
XM_005268629.4:c.6092C>G	XP_005268686.1:p.Thr2031Arg
XM_011537877.3:c.6092C>G	XP_011536179.1:p.Thr2031Arg
XM_017018787.1:c.3008C>G	XP_016874276.1:p.Thr1003Arg
XM_017018788.2:c.2354C>G	XP_016874277.1:p.Thr785Arg
XM_024448833.1:c.4889C>G	XP_024304601.1:p.Thr1630Arg
NM_198578.4:c.6092C>G MANE Select	NP_940980.4:p.Thr2031Arg