Canonical Allele Identifier: CA384419434

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40713811G>T (hg19) ; chr12:g.40320009G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40320009G>T , CM000674.2:g.40320009G>T	GRCh38
NC_000012.11:g.40713811G>T , CM000674.1:g.40713811G>T	GRCh37
NC_000012.10:g.39000078G>T	NCBI36
NG_011709.1:g.99999G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.4849G>T MANE Select	ENSP00000298910.7:p.Gly1617Cys
ENST00000679360.1:c.*3758G>T	ENSP00000505368.1:n.*3758G>T
ENST00000679532.1:c.623G>T
ENST00000680018.1:c.294G>T	ENSP00000505347.1:n.294G>T
ENST00000680422.1:c.494G>T
ENST00000680425.1:c.183-1025G>T	ENSP00000506459.1:n.183-1025G>T
ENST00000680453.1:c.473-1025G>T
ENST00000680790.1:c.4594G>T	ENSP00000505335.1:p.Gly1532Cys
ENST00000681136.1:n.833G>T
ENST00000681696.1:c.532G>T	ENSP00000505871.1:p.Gly178Cys
ENST00000298910.11:c.4849G>T	ENSP00000298910.7:p.Gly1617Cys
ENST00000430804.5:c.2145G>T
ENST00000479187.5:n.1530G>T
ENST00000481256.1:n.508G>T
NM_198578.3:c.4849G>T	NP_940980.3:p.Gly1617Cys
XM_005268629.2:c.4849G>T	XP_005268686.1:p.Gly1617Cys
XM_011537877.1:c.4849G>T	XP_011536179.1:p.Gly1617Cys
XM_011537878.1:c.4849G>T	XP_011536180.1:p.Gly1617Cys
XM_011537879.1:c.3646G>T	XP_011536181.1:p.Gly1216Cys
XM_011537881.1:c.4828-1025G>T	XP_011536183.1:n.4828-1025G>T
XM_005268629.4:c.4849G>T	XP_005268686.1:p.Gly1617Cys
XM_011537877.3:c.4849G>T	XP_011536179.1:p.Gly1617Cys
XM_011537881.3:c.4828-1025G>T	XP_011536183.1:n.4828-1025G>T
XM_017018787.1:c.1765G>T	XP_016874276.1:p.Gly589Cys
XM_017018788.2:c.1111G>T	XP_016874277.1:p.Gly371Cys
XM_024448833.1:c.3646G>T	XP_024304601.1:p.Gly1216Cys
XR_001748574.2:n.5217G>T
NM_198578.4:c.4849G>T MANE Select	NP_940980.4:p.Gly1617Cys