Canonical Allele Identifier: CA2618283249

Gene: LRRK2

Linked Data

• gnomAD v4: 12-40309019-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40309019G>T , CM000674.2:g.40309019G>T	GRCh38
NC_000012.11:g.40702821G>T , CM000674.1:g.40702821G>T	GRCh37
NC_000012.10:g.38989088G>T	NCBI36
NG_011709.1:g.89009G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000298910.12:c.4190-87G>T MANE Select	ENSP00000298910.7:n.4190-87G>T
ENST00000679360.1:c.*3099-87G>T	ENSP00000505368.1:n.*3099-87G>T
ENST00000680790.1:c.3935-87G>T	ENSP00000505335.1:n.3935-87G>T
ENST00000298910.11:c.4190-87G>T	ENSP00000298910.7:n.4190-87G>T
ENST00000430804.5:c.1486-87G>T
ENST00000479187.5:n.871-87G>T
NM_198578.3:c.4190-87G>T	NP_940980.3:n.4190-87G>T
XM_005268629.2:c.4190-87G>T	XP_005268686.1:n.4190-87G>T
XM_011537877.1:c.4190-87G>T	XP_011536179.1:n.4190-87G>T
XM_011537878.1:c.4190-87G>T	XP_011536180.1:n.4190-87G>T
XM_011537879.1:c.2987-87G>T	XP_011536181.1:n.2987-87G>T
XM_011537880.1:c.4190-87G>T	XP_011536182.1:n.4190-87G>T
XM_011537881.1:c.4190-87G>T	XP_011536183.1:n.4190-87G>T
XM_005268629.4:c.4190-87G>T	XP_005268686.1:n.4190-87G>T
XM_011537877.3:c.4190-87G>T	XP_011536179.1:n.4190-87G>T
XM_011537881.3:c.4190-87G>T	XP_011536183.1:n.4190-87G>T
XM_017018786.2:c.4190-87G>T	XP_016874275.1:n.4190-87G>T
XM_017018787.1:c.1106-87G>T	XP_016874276.1:n.1106-87G>T
XM_017018788.2:c.452-87G>T	XP_016874277.1:n.452-87G>T
XM_024448833.1:c.2987-87G>T	XP_024304601.1:n.2987-87G>T
XR_001748574.2:n.4432-87G>T
NM_198578.4:c.4190-87G>T MANE Select	NP_940980.4:n.4190-87G>T