Canonical Allele Identifier: CA2030916205

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40263923_40263924delinsTG , CM000674.2:g.40263923_40263924delinsTG	GRCh38
NC_000012.11:g.40657725_40657726delinsTG , CM000674.1:g.40657725_40657726delinsTG	GRCh37
NC_000012.10:g.38943992_38943993delinsTG	NCBI36
NG_011709.1:g.43913_43914delinsTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000298910.12:c.1656+22_1656+23delinsTG MANE Select	ENSP00000298910.7:n.1656+22_1656+23delins...
ENST00000679360.1:c.*565+22_*565+23delinsTG	ENSP00000505368.1:n.*565+22_*565+23delins...
ENST00000680790.1:c.1401+22_1401+23delinsTG	ENSP00000505335.1:n.1401+22_1401+23delins...
ENST00000298910.11:c.1656+22_1656+23delinsTG	ENSP00000298910.7:n.1656+22_1656+23delins...
ENST00000343742.6:c.1656+22_1656+23delinsTG	ENSP00000341930.2:n.1656+22_1656+23delins...
ENST00000416796.5:c.900+22_900+23delinsTG	ENSP00000398726.1:n.900+22_900+23delinsTG...
NM_198578.3:c.1656+22_1656+23delinsTG	NP_940980.3:n.1656+22_1656+23delinsTG
XM_005268629.2:c.1656+22_1656+23delinsTG	XP_005268686.1:n.1656+22_1656+23delinsTG
XM_011537877.1:c.1656+22_1656+23delinsTG	XP_011536179.1:n.1656+22_1656+23delinsTG
XM_011537878.1:c.1656+22_1656+23delinsTG	XP_011536180.1:n.1656+22_1656+23delinsTG
XM_011537879.1:c.453+22_453+23delinsTG	XP_011536181.1:n.453+22_453+23delinsTG
XM_011537880.1:c.1656+22_1656+23delinsTG	XP_011536182.1:n.1656+22_1656+23delinsTG
XM_011537881.1:c.1656+22_1656+23delinsTG	XP_011536183.1:n.1656+22_1656+23delinsTG
XM_011537882.1:c.1656+22_1656+23delinsTG	XP_011536184.1:n.1656+22_1656+23delinsTG
XM_005268629.4:c.1656+22_1656+23delinsTG	XP_005268686.1:n.1656+22_1656+23delinsTG
XM_011537877.3:c.1656+22_1656+23delinsTG	XP_011536179.1:n.1656+22_1656+23delinsTG
XM_011537881.3:c.1656+22_1656+23delinsTG	XP_011536183.1:n.1656+22_1656+23delinsTG
XM_011537882.3:c.1656+22_1656+23delinsTG	XP_011536184.1:n.1656+22_1656+23delinsTG
XM_017018786.2:c.1656+22_1656+23delinsTG	XP_016874275.1:n.1656+22_1656+23delinsTG
XM_017018789.2:c.1656+22_1656+23delinsTG	XP_016874278.1:n.1656+22_1656+23delinsTG
XM_024448833.1:c.453+22_453+23delinsTG	XP_024304601.1:n.453+22_453+23delinsTG
XR_001748574.2:n.1898+22_1898+23delinsTG
NM_198578.4:c.1656+22_1656+23delinsTG MANE Select	NP_940980.4:n.1656+22_1656+23delinsTG