Canonical Allele Identifier: CA2618286348

Gene: LRRK2

Linked Data

• gnomAD v4: 12-40363277-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40363277A>C , CM000674.2:g.40363277A>C	GRCh38
NC_000012.11:g.40757079A>C , CM000674.1:g.40757079A>C	GRCh37
NC_000012.10:g.39043346A>C	NCBI36
NG_011709.1:g.143267A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000298910.12:c.7029-125A>C MANE Select	ENSP00000298910.7:n.7029-125A>C
ENST00000636518.1:c.826-125A>C
ENST00000679360.1:c.*5938-125A>C	ENSP00000505368.1:n.*5938-125A>C
ENST00000679532.1:c.2803-125A>C
ENST00000679683.1:c.819-125A>C
ENST00000680018.1:c.2474-125A>C	ENSP00000505347.1:n.2474-125A>C
ENST00000680422.1:c.4116-125A>C
ENST00000680425.1:c.2196-125A>C	ENSP00000506459.1:n.2196-125A>C
ENST00000680453.1:c.2486-125A>C
ENST00000680790.1:c.6774-125A>C	ENSP00000505335.1:n.6774-125A>C
ENST00000681136.1:n.3013-125A>C
ENST00000681696.1:c.2712-125A>C	ENSP00000505871.1:n.2712-125A>C
ENST00000681773.1:n.236-125A>C
ENST00000298910.11:c.7029-125A>C	ENSP00000298910.7:n.7029-125A>C
ENST00000430804.5:c.4325-125A>C
ENST00000479187.5:n.3710-125A>C
NM_198578.3:c.7029-125A>C	NP_940980.3:n.7029-125A>C
XM_005268629.2:c.7029-125A>C	XP_005268686.1:n.7029-125A>C
XM_011537877.1:c.7029-125A>C	XP_011536179.1:n.7029-125A>C
XM_011537878.1:c.*752A>C	XP_011536180.1:n.*752A>C
XM_011537879.1:c.5826-125A>C	XP_011536181.1:n.5826-125A>C
XR_944868.1:n.485-8450T>G
XM_005268629.4:c.7029-125A>C	XP_005268686.1:n.7029-125A>C
XM_011537877.3:c.7029-125A>C	XP_011536179.1:n.7029-125A>C
XM_017018787.1:c.3945-125A>C	XP_016874276.1:n.3945-125A>C
XM_017018788.2:c.3291-125A>C	XP_016874277.1:n.3291-125A>C
XM_024448833.1:c.5826-125A>C	XP_024304601.1:n.5826-125A>C
XR_944868.2:n.485-8450T>G
NM_198578.4:c.7029-125A>C MANE Select	NP_940980.4:n.7029-125A>C