Canonical Allele Identifier: CA604504350

Gene: LRRK2

Linked Data

• dbSNP Id: rs1262771121
• gnomAD v2: 12-40716882-AT-A
• gnomAD v3: 12-40323080-AT-A
• gnomAD v4: 12-40323080-AT-A
• MyVariant Identifiers: chr12:g.40716883del (hg19) ; chr12:g.40323081del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40323086del , CM000674.2:g.40323086del	GRCh38
NC_000012.11:g.40716888del , CM000674.1:g.40716888del	GRCh37
NC_000012.10:g.39003155del	NCBI36
NG_011709.1:g.103076del

Transcript Alleles

HGVS	Amino-acid change
ENST00000298910.12:c.5510-74del MANE Select	ENSP00000298910.7:n.5510-74del
ENST00000679360.1:c.*4419-74del	ENSP00000505368.1:n.*4419-74del
ENST00000679532.1:c.1284-74del
ENST00000680018.1:c.955-74del	ENSP00000505347.1:n.955-74del
ENST00000680422.1:c.1155-74del
ENST00000680425.1:c.677-74del	ENSP00000506459.1:n.677-74del
ENST00000680453.1:c.967-74del
ENST00000680790.1:c.5255-74del	ENSP00000505335.1:n.5255-74del
ENST00000681136.1:n.1494-74del
ENST00000681696.1:c.1193-74del	ENSP00000505871.1:n.1193-74del
ENST00000298910.11:c.5510-74del	ENSP00000298910.7:n.5510-74del
ENST00000430804.5:c.2806-74del
ENST00000479187.5:n.2191-74del
NM_198578.3:c.5510-74del	NP_940980.3:n.5510-74del
XM_005268629.2:c.5510-74del	XP_005268686.1:n.5510-74del
XM_011537877.1:c.5510-74del	XP_011536179.1:n.5510-74del
XM_011537878.1:c.5510-74del	XP_011536180.1:n.5510-74del
XM_011537879.1:c.4307-74del	XP_011536181.1:n.4307-74del
XM_005268629.4:c.5510-74del	XP_005268686.1:n.5510-74del
XM_011537877.3:c.5510-74del	XP_011536179.1:n.5510-74del
XM_017018787.1:c.2426-74del	XP_016874276.1:n.2426-74del
XM_017018788.2:c.1772-74del	XP_016874277.1:n.1772-74del
XM_024448833.1:c.4307-74del	XP_024304601.1:n.4307-74del
NM_198578.4:c.5510-74del MANE Select	NP_940980.4:n.5510-74del