Canonical Allele Identifier: CA384413281

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40757256A>T (hg19) ; chr12:g.40363454A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40363454A>T , CM000674.2:g.40363454A>T	GRCh38
NC_000012.11:g.40757256A>T , CM000674.1:g.40757256A>T	GRCh37
NC_000012.10:g.39043523A>T	NCBI36
NG_011709.1:g.143444A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.7081A>T MANE Select	ENSP00000298910.7:p.Thr2361Ser
ENST00000636518.1:c.878A>T
ENST00000679360.1:c.*5990A>T	ENSP00000505368.1:n.*5990A>T
ENST00000679532.1:c.2855A>T
ENST00000679683.1:c.871A>T
ENST00000680018.1:c.2526A>T	ENSP00000505347.1:n.2526A>T
ENST00000680422.1:c.4168A>T
ENST00000680425.1:c.2248A>T	ENSP00000506459.1:n.2248A>T
ENST00000680453.1:c.2538A>T
ENST00000680790.1:c.6826A>T	ENSP00000505335.1:p.Thr2276Ser
ENST00000681136.1:n.3065A>T
ENST00000681696.1:c.2764A>T	ENSP00000505871.1:p.Thr922Ser
ENST00000681773.1:n.288A>T
ENST00000298910.11:c.7081A>T	ENSP00000298910.7:p.Thr2361Ser
ENST00000430804.5:c.4377A>T
ENST00000479187.5:n.3762A>T
NM_198578.3:c.7081A>T	NP_940980.3:p.Thr2361Ser
XM_005268629.2:c.7081A>T	XP_005268686.1:p.Thr2361Ser
XM_011537877.1:c.7081A>T	XP_011536179.1:p.Thr2361Ser
XM_011537879.1:c.5878A>T	XP_011536181.1:p.Thr1960Ser
XR_944868.1:n.485-8627T>A
XM_005268629.4:c.7081A>T	XP_005268686.1:p.Thr2361Ser
XM_011537877.3:c.7081A>T	XP_011536179.1:p.Thr2361Ser
XM_017018787.1:c.3997A>T	XP_016874276.1:p.Thr1333Ser
XM_017018788.2:c.3343A>T	XP_016874277.1:p.Thr1115Ser
XM_024448833.1:c.5878A>T	XP_024304601.1:p.Thr1960Ser
XR_944868.2:n.485-8627T>A
NM_198578.4:c.7081A>T MANE Select	NP_940980.4:p.Thr2361Ser