Canonical Allele Identifier: CA384403700

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40734144T>G (hg19) ; chr12:g.40340342T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40340342T>G , CM000674.2:g.40340342T>G	GRCh38
NC_000012.11:g.40734144T>G , CM000674.1:g.40734144T>G	GRCh37
NC_000012.10:g.39020411T>G	NCBI36
NG_011709.1:g.120332T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.5997T>G MANE Select	ENSP00000298910.7:p.Asn1999Lys
ENST00000679360.1:c.*4906T>G	ENSP00000505368.1:n.*4906T>G
ENST00000679532.1:c.1771T>G
ENST00000680018.1:c.1442T>G	ENSP00000505347.1:n.1442T>G
ENST00000680422.1:c.1642T>G
ENST00000680425.1:c.1164T>G	ENSP00000506459.1:n.1164T>G
ENST00000680453.1:c.1454T>G
ENST00000680790.1:c.5742T>G	ENSP00000505335.1:p.Asn1914Lys
ENST00000681136.1:n.1981T>G
ENST00000681696.1:c.1680T>G	ENSP00000505871.1:p.Asn560Lys
ENST00000298910.11:c.5997T>G	ENSP00000298910.7:p.Asn1999Lys
ENST00000430804.5:c.3293T>G
ENST00000479187.5:n.2678T>G
NM_198578.3:c.5997T>G	NP_940980.3:p.Asn1999Lys
XM_005268629.2:c.5997T>G	XP_005268686.1:p.Asn1999Lys
XM_011537877.1:c.5997T>G	XP_011536179.1:p.Asn1999Lys
XM_011537878.1:c.5997T>G	XP_011536180.1:p.Asn1999Lys
XM_011537879.1:c.4794T>G	XP_011536181.1:p.Asn1598Lys
XM_005268629.4:c.5997T>G	XP_005268686.1:p.Asn1999Lys
XM_011537877.3:c.5997T>G	XP_011536179.1:p.Asn1999Lys
XM_017018787.1:c.2913T>G	XP_016874276.1:p.Asn971Lys
XM_017018788.2:c.2259T>G	XP_016874277.1:p.Asn753Lys
XM_024448833.1:c.4794T>G	XP_024304601.1:p.Asn1598Lys
NM_198578.4:c.5997T>G MANE Select	NP_940980.4:p.Asn1999Lys