Canonical Allele Identifier: CA604810407

Gene: LRRK2

Linked Data

• dbSNP Id: rs1413648954
• gnomAD v2: 12-40702653-CA-C
• gnomAD v3: 12-40308851-CA-C
• gnomAD v4: 12-40308851-CA-C
• MyVariant Identifiers: chr12:g.40702654del (hg19) ; chr12:g.40308852del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40308852del , CM000674.2:g.40308852del	GRCh38
NC_000012.11:g.40702654del , CM000674.1:g.40702654del	GRCh37
NC_000012.10:g.38988921del	NCBI36
NG_011709.1:g.88842del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.4189+156del MANE Select	ENSP00000298910.7:n.4189+156del
ENST00000679360.1:c.*3098+156del	ENSP00000505368.1:n.*3098+156del
ENST00000680790.1:c.3934+156del	ENSP00000505335.1:n.3934+156del
ENST00000298910.11:c.4189+156del	ENSP00000298910.7:n.4189+156del
ENST00000430804.5:c.1485+156del
ENST00000479187.5:n.870+156del
NM_198578.3:c.4189+156del	NP_940980.3:n.4189+156del
XM_005268629.2:c.4189+156del	XP_005268686.1:n.4189+156del
XM_011537877.1:c.4189+156del	XP_011536179.1:n.4189+156del
XM_011537878.1:c.4189+156del	XP_011536180.1:n.4189+156del
XM_011537879.1:c.2986+156del	XP_011536181.1:n.2986+156del
XM_011537880.1:c.4189+156del	XP_011536182.1:n.4189+156del
XM_011537881.1:c.4189+156del	XP_011536183.1:n.4189+156del
XM_005268629.4:c.4189+156del	XP_005268686.1:n.4189+156del
XM_011537877.3:c.4189+156del	XP_011536179.1:n.4189+156del
XM_011537881.3:c.4189+156del	XP_011536183.1:n.4189+156del
XM_017018786.2:c.4189+156del	XP_016874275.1:n.4189+156del
XM_017018787.1:c.1105+156del	XP_016874276.1:n.1105+156del
XM_017018788.2:c.451+156del	XP_016874277.1:n.451+156del
XM_024448833.1:c.2986+156del	XP_024304601.1:n.2986+156del
XR_001748574.2:n.4431+156del
NM_198578.4:c.4189+156del MANE Select	NP_940980.4:n.4189+156del