Canonical Allele Identifier: CA919070295

Gene: LRRK2

Linked Data

• dbSNP Id: rs1592283717
• gnomAD v4: 12-40320301-ACCT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40320305_40320307del , CM000674.2:g.40320305_40320307del	GRCh38
NC_000012.11:g.40714107_40714109del , CM000674.1:g.40714107_40714109del	GRCh37
NC_000012.10:g.39000374_39000376del	NCBI36
NG_011709.1:g.100295_100297del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.5015+130_5015+132del MANE Select	ENSP00000298910.7:n.5015+130_5015+132del
ENST00000679360.1:c.*3924+130_*3924+132del	ENSP00000505368.1:n.*3924+130_*3924+132del
ENST00000679532.1:c.789+130_789+132del
ENST00000680018.1:c.460+130_460+132del	ENSP00000505347.1:n.460+130_460+132del
ENST00000680422.1:c.660+130_660+132del
ENST00000680425.1:c.183-729_183-727del	ENSP00000506459.1:n.183-729_183-727del
ENST00000680453.1:c.473-729_473-727del
ENST00000680790.1:c.4760+130_4760+132del	ENSP00000505335.1:n.4760+130_4760+132del
ENST00000681136.1:n.999+130_999+132del
ENST00000681696.1:c.698+130_698+132del	ENSP00000505871.1:n.698+130_698+132del
ENST00000298910.11:c.5015+130_5015+132del	ENSP00000298910.7:n.5015+130_5015+132del
ENST00000430804.5:c.2311+130_2311+132del
ENST00000479187.5:n.1696+130_1696+132del
NM_198578.3:c.5015+130_5015+132del	NP_940980.3:n.5015+130_5015+132del
XM_005268629.2:c.5015+130_5015+132del	XP_005268686.1:n.5015+130_5015+132del
XM_011537877.1:c.5015+130_5015+132del	XP_011536179.1:n.5015+130_5015+132del
XM_011537878.1:c.5015+130_5015+132del	XP_011536180.1:n.5015+130_5015+132del
XM_011537879.1:c.3812+130_3812+132del	XP_011536181.1:n.3812+130_3812+132del
XM_011537881.1:c.4828-729_4828-727del	XP_011536183.1:n.4828-729_4828-727del
XM_005268629.4:c.5015+130_5015+132del	XP_005268686.1:n.5015+130_5015+132del
XM_011537877.3:c.5015+130_5015+132del	XP_011536179.1:n.5015+130_5015+132del
XM_011537881.3:c.4828-729_4828-727del	XP_011536183.1:n.4828-729_4828-727del
XM_017018787.1:c.1931+130_1931+132del	XP_016874276.1:n.1931+130_1931+132del
XM_017018788.2:c.1277+130_1277+132del	XP_016874277.1:n.1277+130_1277+132del
XM_024448833.1:c.3812+130_3812+132del	XP_024304601.1:n.3812+130_3812+132del
XR_001748574.2:n.5383+130_5383+132del
NM_198578.4:c.5015+130_5015+132del MANE Select	NP_940980.4:n.5015+130_5015+132del