Canonical Allele Identifier: CA384413441

Gene: LRRK2

Linked Data

• gnomAD v4: 12-40363499-T-C
• MyVariant Identifiers: chr12:g.40757301T>C (hg19) ; chr12:g.40363499T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40363499T>C , CM000674.2:g.40363499T>C	GRCh38
NC_000012.11:g.40757301T>C , CM000674.1:g.40757301T>C	GRCh37
NC_000012.10:g.39043568T>C	NCBI36
NG_011709.1:g.143489T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.7126T>C MANE Select	ENSP00000298910.7:p.Trp2376Arg
ENST00000636518.1:c.923T>C
ENST00000679360.1:c.*6035T>C	ENSP00000505368.1:n.*6035T>C
ENST00000679532.1:c.2900T>C
ENST00000679683.1:c.916T>C
ENST00000680018.1:c.2571T>C	ENSP00000505347.1:n.2571T>C
ENST00000680422.1:c.4213T>C
ENST00000680425.1:c.2293T>C	ENSP00000506459.1:n.2293T>C
ENST00000680453.1:c.2583T>C
ENST00000680790.1:c.6871T>C	ENSP00000505335.1:p.Trp2291Arg
ENST00000681136.1:n.3110T>C
ENST00000681696.1:c.2809T>C	ENSP00000505871.1:p.Trp937Arg
ENST00000681773.1:n.333T>C
ENST00000298910.11:c.7126T>C	ENSP00000298910.7:p.Trp2376Arg
ENST00000430804.5:c.4422T>C
ENST00000479187.5:n.3807T>C
NM_198578.3:c.7126T>C	NP_940980.3:p.Trp2376Arg
XM_005268629.2:c.7126T>C	XP_005268686.1:p.Trp2376Arg
XM_011537877.1:c.7126T>C	XP_011536179.1:p.Trp2376Arg
XM_011537879.1:c.5923T>C	XP_011536181.1:p.Trp1975Arg
XR_944868.1:n.485-8672A>G
XM_005268629.4:c.7126T>C	XP_005268686.1:p.Trp2376Arg
XM_011537877.3:c.7126T>C	XP_011536179.1:p.Trp2376Arg
XM_017018787.1:c.4042T>C	XP_016874276.1:p.Trp1348Arg
XM_017018788.2:c.3388T>C	XP_016874277.1:p.Trp1130Arg
XM_024448833.1:c.5923T>C	XP_024304601.1:p.Trp1975Arg
XR_944868.2:n.485-8672A>G
NM_198578.4:c.7126T>C MANE Select	NP_940980.4:p.Trp2376Arg