Canonical Allele Identifier: CA384413392

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40757286C>G (hg19) ; chr12:g.40363484C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40363484C>G , CM000674.2:g.40363484C>G	GRCh38
NC_000012.11:g.40757286C>G , CM000674.1:g.40757286C>G	GRCh37
NC_000012.10:g.39043553C>G	NCBI36
NG_011709.1:g.143474C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.7111C>G MANE Select	ENSP00000298910.7:p.Pro2371Ala
ENST00000636518.1:c.908C>G
ENST00000679360.1:c.*6020C>G	ENSP00000505368.1:n.*6020C>G
ENST00000679532.1:c.2885C>G
ENST00000679683.1:c.901C>G
ENST00000680018.1:c.2556C>G	ENSP00000505347.1:n.2556C>G
ENST00000680422.1:c.4198C>G
ENST00000680425.1:c.2278C>G	ENSP00000506459.1:n.2278C>G
ENST00000680453.1:c.2568C>G
ENST00000680790.1:c.6856C>G	ENSP00000505335.1:p.Pro2286Ala
ENST00000681136.1:n.3095C>G
ENST00000681696.1:c.2794C>G	ENSP00000505871.1:p.Pro932Ala
ENST00000681773.1:n.318C>G
ENST00000298910.11:c.7111C>G	ENSP00000298910.7:p.Pro2371Ala
ENST00000430804.5:c.4407C>G
ENST00000479187.5:n.3792C>G
NM_198578.3:c.7111C>G	NP_940980.3:p.Pro2371Ala
XM_005268629.2:c.7111C>G	XP_005268686.1:p.Pro2371Ala
XM_011537877.1:c.7111C>G	XP_011536179.1:p.Pro2371Ala
XM_011537879.1:c.5908C>G	XP_011536181.1:p.Pro1970Ala
XR_944868.1:n.485-8657G>C
XM_005268629.4:c.7111C>G	XP_005268686.1:p.Pro2371Ala
XM_011537877.3:c.7111C>G	XP_011536179.1:p.Pro2371Ala
XM_017018787.1:c.4027C>G	XP_016874276.1:p.Pro1343Ala
XM_017018788.2:c.3373C>G	XP_016874277.1:p.Pro1125Ala
XM_024448833.1:c.5908C>G	XP_024304601.1:p.Pro1970Ala
XR_944868.2:n.485-8657G>C
NM_198578.4:c.7111C>G MANE Select	NP_940980.4:p.Pro2371Ala