Canonical Allele Identifier: CA479238749

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40734210T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40340408T>A , CM000674.2:g.40340408T>A	GRCh38
NC_000012.11:g.40734210T>A , CM000674.1:g.40734210T>A	GRCh37
NC_000012.10:g.39020477T>A	NCBI36
NG_011709.1:g.120398T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000298910.12:c.6063T>A MANE Select	ENSP00000298910.7:p.Ala2021=
ENST00000679360.1:c.*4972T>A	ENSP00000505368.1:n.*4972T>A
ENST00000679532.1:c.1837T>A
ENST00000680018.1:c.1508T>A	ENSP00000505347.1:n.1508T>A
ENST00000680422.1:c.1708T>A
ENST00000680425.1:c.1230T>A	ENSP00000506459.1:n.1230T>A
ENST00000680453.1:c.1520T>A
ENST00000680790.1:c.5808T>A	ENSP00000505335.1:p.Ala1936=
ENST00000681136.1:n.2047T>A
ENST00000681696.1:c.1746T>A	ENSP00000505871.1:p.Ala582=
ENST00000298910.11:c.6063T>A	ENSP00000298910.7:p.Ala2021=
ENST00000430804.5:c.3359T>A
ENST00000479187.5:n.2744T>A
NM_198578.3:c.6063T>A	NP_940980.3:p.Ala2021=
XM_005268629.2:c.6063T>A	XP_005268686.1:p.Ala2021=
XM_011537877.1:c.6063T>A	XP_011536179.1:p.Ala2021=
XM_011537878.1:c.6063T>A	XP_011536180.1:p.Ala2021=
XM_011537879.1:c.4860T>A	XP_011536181.1:p.Ala1620=
XM_005268629.4:c.6063T>A	XP_005268686.1:p.Ala2021=
XM_011537877.3:c.6063T>A	XP_011536179.1:p.Ala2021=
XM_017018787.1:c.2979T>A	XP_016874276.1:p.Ala993=
XM_017018788.2:c.2325T>A	XP_016874277.1:p.Ala775=
XM_024448833.1:c.4860T>A	XP_024304601.1:p.Ala1620=
NM_198578.4:c.6063T>A MANE Select	NP_940980.4:p.Ala2021=