Canonical Allele Identifier: CA2595182508

Gene: LRRK2

Linked Data

• dbSNP Id: rs2136953880
• gnomAD v3: 12-40340126-CTT-C
• gnomAD v4: 12-40340126-CTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40340127_40340128del , CM000674.2:g.40340127_40340128del	GRCh38
NC_000012.11:g.40733929_40733930del , CM000674.1:g.40733929_40733930del	GRCh37
NC_000012.10:g.39020196_39020197del	NCBI36
NG_011709.1:g.120117_120118del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.5949-167_5949-166del MANE Select	ENSP00000298910.7:n.5949-167_5949-166del
ENST00000679360.1:c.*4858-167_*4858-166del	ENSP00000505368.1:n.*4858-167_*4858-166del
ENST00000679532.1:c.1723-167_1723-166del
ENST00000680018.1:c.1394-167_1394-166del	ENSP00000505347.1:n.1394-167_1394-166del
ENST00000680422.1:c.1594-167_1594-166del
ENST00000680425.1:c.1116-167_1116-166del	ENSP00000506459.1:n.1116-167_1116-166del
ENST00000680453.1:c.1406-167_1406-166del
ENST00000680790.1:c.5694-167_5694-166del	ENSP00000505335.1:n.5694-167_5694-166del
ENST00000681136.1:n.1933-167_1933-166del
ENST00000681696.1:c.1632-167_1632-166del	ENSP00000505871.1:n.1632-167_1632-166del
ENST00000298910.11:c.5949-167_5949-166del	ENSP00000298910.7:n.5949-167_5949-166del
ENST00000430804.5:c.3245-167_3245-166del
ENST00000479187.5:n.2630-167_2630-166del
NM_198578.3:c.5949-167_5949-166del	NP_940980.3:n.5949-167_5949-166del
XM_005268629.2:c.5949-167_5949-166del	XP_005268686.1:n.5949-167_5949-166del
XM_011537877.1:c.5949-167_5949-166del	XP_011536179.1:n.5949-167_5949-166del
XM_011537878.1:c.5949-167_5949-166del	XP_011536180.1:n.5949-167_5949-166del
XM_011537879.1:c.4746-167_4746-166del	XP_011536181.1:n.4746-167_4746-166del
XM_005268629.4:c.5949-167_5949-166del	XP_005268686.1:n.5949-167_5949-166del
XM_011537877.3:c.5949-167_5949-166del	XP_011536179.1:n.5949-167_5949-166del
XM_017018787.1:c.2865-167_2865-166del	XP_016874276.1:n.2865-167_2865-166del
XM_017018788.2:c.2211-167_2211-166del	XP_016874277.1:n.2211-167_2211-166del
XM_024448833.1:c.4746-167_4746-166del	XP_024304601.1:n.4746-167_4746-166del
NM_198578.4:c.5949-167_5949-166del MANE Select	NP_940980.4:n.5949-167_5949-166del