Canonical Allele Identifier: CA384413350

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40757276G>T (hg19) ; chr12:g.40363474G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40363474G>T , CM000674.2:g.40363474G>T	GRCh38
NC_000012.11:g.40757276G>T , CM000674.1:g.40757276G>T	GRCh37
NC_000012.10:g.39043543G>T	NCBI36
NG_011709.1:g.143464G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.7101G>T MANE Select	ENSP00000298910.7:p.Lys2367Asn
ENST00000636518.1:c.898G>T
ENST00000679360.1:c.*6010G>T	ENSP00000505368.1:n.*6010G>T
ENST00000679532.1:c.2875G>T
ENST00000679683.1:c.891G>T
ENST00000680018.1:c.2546G>T	ENSP00000505347.1:n.2546G>T
ENST00000680422.1:c.4188G>T
ENST00000680425.1:c.2268G>T	ENSP00000506459.1:n.2268G>T
ENST00000680453.1:c.2558G>T
ENST00000680790.1:c.6846G>T	ENSP00000505335.1:p.Lys2282Asn
ENST00000681136.1:n.3085G>T
ENST00000681696.1:c.2784G>T	ENSP00000505871.1:p.Lys928Asn
ENST00000681773.1:n.308G>T
ENST00000298910.11:c.7101G>T	ENSP00000298910.7:p.Lys2367Asn
ENST00000430804.5:c.4397G>T
ENST00000479187.5:n.3782G>T
NM_198578.3:c.7101G>T	NP_940980.3:p.Lys2367Asn
XM_005268629.2:c.7101G>T	XP_005268686.1:p.Lys2367Asn
XM_011537877.1:c.7101G>T	XP_011536179.1:p.Lys2367Asn
XM_011537879.1:c.5898G>T	XP_011536181.1:p.Lys1966Asn
XR_944868.1:n.485-8647C>A
XM_005268629.4:c.7101G>T	XP_005268686.1:p.Lys2367Asn
XM_011537877.3:c.7101G>T	XP_011536179.1:p.Lys2367Asn
XM_017018787.1:c.4017G>T	XP_016874276.1:p.Lys1339Asn
XM_017018788.2:c.3363G>T	XP_016874277.1:p.Lys1121Asn
XM_024448833.1:c.5898G>T	XP_024304601.1:p.Lys1966Asn
XR_944868.2:n.485-8647C>A
NM_198578.4:c.7101G>T MANE Select	NP_940980.4:p.Lys2367Asn