Canonical Allele Identifier: CA604490053

Gene: LRRK2

Linked Data

• dbSNP Id: rs1263892751
• gnomAD v2: 12-40620702-ACT-A
• gnomAD v3: 12-40226900-ACT-A
• gnomAD v4: 12-40226900-ACT-A
• MyVariant Identifiers: chr12:g.40620703_40620704del (hg19) ; chr12:g.40226901_40226902del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40226903_40226904del , CM000674.2:g.40226903_40226904del	GRCh38
NC_000012.11:g.40620705_40620706del , CM000674.1:g.40620705_40620706del	GRCh37
NC_000012.10:g.38906972_38906973del	NCBI36
NG_011709.1:g.6893_6894del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.237+1263_237+1264del MANE Select	ENSP00000298910.7:n.237+1263_237+1264del
ENST00000644108.1:c.182-988_182-987del
ENST00000679360.1:c.237+1263_237+1264del	ENSP00000505368.1:n.237+1263_237+1264del
ENST00000680235.1:n.392+1263_392+1264del
ENST00000680790.1:c.237+1263_237+1264del	ENSP00000505335.1:n.237+1263_237+1264del
ENST00000298910.11:c.237+1263_237+1264del	ENSP00000298910.7:n.237+1263_237+1264del
ENST00000343742.6:c.237+1263_237+1264del	ENSP00000341930.2:n.237+1263_237+1264del
ENST00000416796.5:c.24+1263_24+1264del	ENSP00000398726.1:n.24+1263_24+1264del
ENST00000474202.1:n.46+1263_46+1264del
NM_198578.3:c.237+1263_237+1264del	NP_940980.3:n.237+1263_237+1264del
XM_005268629.2:c.237+1263_237+1264del	XP_005268686.1:n.237+1263_237+1264del
XM_011537877.1:c.237+1263_237+1264del	XP_011536179.1:n.237+1263_237+1264del
XM_011537878.1:c.237+1263_237+1264del	XP_011536180.1:n.237+1263_237+1264del
XM_011537880.1:c.237+1263_237+1264del	XP_011536182.1:n.237+1263_237+1264del
XM_011537881.1:c.237+1263_237+1264del	XP_011536183.1:n.237+1263_237+1264del
XM_011537882.1:c.237+1263_237+1264del	XP_011536184.1:n.237+1263_237+1264del
XM_005268629.4:c.237+1263_237+1264del	XP_005268686.1:n.237+1263_237+1264del
XM_011537877.3:c.237+1263_237+1264del	XP_011536179.1:n.237+1263_237+1264del
XM_011537881.3:c.237+1263_237+1264del	XP_011536183.1:n.237+1263_237+1264del
XM_011537882.3:c.237+1263_237+1264del	XP_011536184.1:n.237+1263_237+1264del
XM_017018786.2:c.237+1263_237+1264del	XP_016874275.1:n.237+1263_237+1264del
XM_017018789.2:c.237+1263_237+1264del	XP_016874278.1:n.237+1263_237+1264del
XR_001748574.2:n.479+1263_479+1264del
NM_198578.4:c.237+1263_237+1264del MANE Select	NP_940980.4:n.237+1263_237+1264del