Canonical Allele Identifier: CA384411793

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40359354A>G , CM000674.2:g.40359354A>G	GRCh38
NC_000012.11:g.40753156A>G , CM000674.1:g.40753156A>G	GRCh37
NC_000012.10:g.39039423A>G	NCBI36
NG_011709.1:g.139344A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_198578.4:c.6938A>G MANE Select	NP_940980.4:p.Asn2313Ser
ENST00000298910.12:c.6938A>G MANE Select	ENSP00000298910.7:p.Asn2313Ser
NM_198578.3:c.6938A>G	NP_940980.3:p.Asn2313Ser
ENST00000298910.11:c.6938A>G	ENSP00000298910.7:p.Asn2313Ser
ENST00000430804.5:c.4234A>G
ENST00000479187.5:n.3619A>G
ENST00000636518.1:c.735A>G
ENST00000679360.1:c.*5847A>G	ENSP00000505368.1:n.*5847A>G
ENST00000679532.1:c.2712A>G
ENST00000679683.1:c.728A>G
ENST00000680018.1:c.2383A>G	ENSP00000505347.1:n.2383A>G
ENST00000680422.1:c.4025A>G
ENST00000680425.1:c.2105A>G	ENSP00000506459.1:n.2105A>G
ENST00000680453.1:c.2395A>G
ENST00000680790.1:c.6683A>G	ENSP00000505335.1:p.Asn2228Ser
ENST00000681136.1:n.2922A>G
ENST00000681696.1:c.2621A>G	ENSP00000505871.1:p.Asn874Ser
ENST00000681773.1:n.145A>G
XM_005268629.2:c.6938A>G	XP_005268686.1:p.Asn2313Ser
XM_005268629.4:c.6938A>G	XP_005268686.1:p.Asn2313Ser
XM_011537877.1:c.6938A>G	XP_011536179.1:p.Asn2313Ser
XM_011537877.3:c.6938A>G	XP_011536179.1:p.Asn2313Ser
XM_011537878.1:c.6938A>G	XP_011536180.1:p.Asn2313Ser
XM_011537879.1:c.5735A>G	XP_011536181.1:p.Asn1912Ser
XM_017018787.1:c.3854A>G	XP_016874276.1:p.Asn1285Ser
XM_017018788.2:c.3200A>G	XP_016874277.1:p.Asn1067Ser
XM_024448833.1:c.5735A>G	XP_024304601.1:p.Asn1912Ser
XR_944868.1:n.485-4527T>C
XR_944868.2:n.485-4527T>C