Canonical Allele Identifier: CA2618284251

Gene: LRRK2

Linked Data

• gnomAD v4: 12-40320224-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40320224A>T , CM000674.2:g.40320224A>T	GRCh38
NC_000012.11:g.40714026A>T , CM000674.1:g.40714026A>T	GRCh37
NC_000012.10:g.39000293A>T	NCBI36
NG_011709.1:g.100214A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.5015+49A>T MANE Select	ENSP00000298910.7:n.5015+49A>T
ENST00000679360.1:c.*3924+49A>T	ENSP00000505368.1:n.*3924+49A>T
ENST00000679532.1:c.789+49A>T
ENST00000680018.1:c.460+49A>T	ENSP00000505347.1:n.460+49A>T
ENST00000680422.1:c.660+49A>T
ENST00000680425.1:c.183-810A>T	ENSP00000506459.1:n.183-810A>T
ENST00000680453.1:c.473-810A>T
ENST00000680790.1:c.4760+49A>T	ENSP00000505335.1:n.4760+49A>T
ENST00000681136.1:n.999+49A>T
ENST00000681696.1:c.698+49A>T	ENSP00000505871.1:n.698+49A>T
ENST00000298910.11:c.5015+49A>T	ENSP00000298910.7:n.5015+49A>T
ENST00000430804.5:c.2311+49A>T
ENST00000479187.5:n.1696+49A>T
NM_198578.3:c.5015+49A>T	NP_940980.3:n.5015+49A>T
XM_005268629.2:c.5015+49A>T	XP_005268686.1:n.5015+49A>T
XM_011537877.1:c.5015+49A>T	XP_011536179.1:n.5015+49A>T
XM_011537878.1:c.5015+49A>T	XP_011536180.1:n.5015+49A>T
XM_011537879.1:c.3812+49A>T	XP_011536181.1:n.3812+49A>T
XM_011537881.1:c.4828-810A>T	XP_011536183.1:n.4828-810A>T
XM_005268629.4:c.5015+49A>T	XP_005268686.1:n.5015+49A>T
XM_011537877.3:c.5015+49A>T	XP_011536179.1:n.5015+49A>T
XM_011537881.3:c.4828-810A>T	XP_011536183.1:n.4828-810A>T
XM_017018787.1:c.1931+49A>T	XP_016874276.1:n.1931+49A>T
XM_017018788.2:c.1277+49A>T	XP_016874277.1:n.1277+49A>T
XM_024448833.1:c.3812+49A>T	XP_024304601.1:n.3812+49A>T
XR_001748574.2:n.5383+49A>T
NM_198578.4:c.5015+49A>T MANE Select	NP_940980.4:n.5015+49A>T