Canonical Allele Identifier: CA2618284296

Gene: LRRK2

Linked Data

• gnomAD v4: 12-40320327-TTTGG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40320328_40320331del , CM000674.2:g.40320328_40320331del	GRCh38
NC_000012.11:g.40714130_40714133del , CM000674.1:g.40714130_40714133del	GRCh37
NC_000012.10:g.39000397_39000400del	NCBI36
NG_011709.1:g.100318_100321del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.5015+153_5015+156del MANE Select	ENSP00000298910.7:n.5015+153_5015+156del
ENST00000679360.1:c.*3924+153_*3924+156del	ENSP00000505368.1:n.*3924+153_*3924+156del
ENST00000679532.1:c.789+153_789+156del
ENST00000680018.1:c.460+153_460+156del	ENSP00000505347.1:n.460+153_460+156del
ENST00000680422.1:c.660+153_660+156del
ENST00000680425.1:c.183-706_183-703del	ENSP00000506459.1:n.183-706_183-703del
ENST00000680453.1:c.473-706_473-703del
ENST00000680790.1:c.4760+153_4760+156del	ENSP00000505335.1:n.4760+153_4760+156del
ENST00000681136.1:n.999+153_999+156del
ENST00000681696.1:c.698+153_698+156del	ENSP00000505871.1:n.698+153_698+156del
ENST00000298910.11:c.5015+153_5015+156del	ENSP00000298910.7:n.5015+153_5015+156del
ENST00000430804.5:c.2311+153_2311+156del
ENST00000479187.5:n.1696+153_1696+156del
NM_198578.3:c.5015+153_5015+156del	NP_940980.3:n.5015+153_5015+156del
XM_005268629.2:c.5015+153_5015+156del	XP_005268686.1:n.5015+153_5015+156del
XM_011537877.1:c.5015+153_5015+156del	XP_011536179.1:n.5015+153_5015+156del
XM_011537878.1:c.5015+153_5015+156del	XP_011536180.1:n.5015+153_5015+156del
XM_011537879.1:c.3812+153_3812+156del	XP_011536181.1:n.3812+153_3812+156del
XM_011537881.1:c.4828-706_4828-703del	XP_011536183.1:n.4828-706_4828-703del
XM_005268629.4:c.5015+153_5015+156del	XP_005268686.1:n.5015+153_5015+156del
XM_011537877.3:c.5015+153_5015+156del	XP_011536179.1:n.5015+153_5015+156del
XM_011537881.3:c.4828-706_4828-703del	XP_011536183.1:n.4828-706_4828-703del
XM_017018787.1:c.1931+153_1931+156del	XP_016874276.1:n.1931+153_1931+156del
XM_017018788.2:c.1277+153_1277+156del	XP_016874277.1:n.1277+153_1277+156del
XM_024448833.1:c.3812+153_3812+156del	XP_024304601.1:n.3812+153_3812+156del
XR_001748574.2:n.5383+153_5383+156del
NM_198578.4:c.5015+153_5015+156del MANE Select	NP_940980.4:n.5015+153_5015+156del