Canonical Allele Identifier: CA2618286466

Gene: LRRK2

Linked Data

• gnomAD v4: 12-40363635-CTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40363637_40363638del , CM000674.2:g.40363637_40363638del	GRCh38
NC_000012.11:g.40757439_40757440del , CM000674.1:g.40757439_40757440del	GRCh37
NC_000012.10:g.39043706_39043707del	NCBI36
NG_011709.1:g.143627_143628del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.7181+83_7181+84del MANE Select	ENSP00000298910.7:n.7181+83_7181+84del
ENST00000636518.1:c.978+83_978+84del
ENST00000679360.1:c.*6090+83_*6090+84del	ENSP00000505368.1:n.*6090+83_*6090+84del
ENST00000679532.1:c.2955+83_2955+84del
ENST00000679683.1:c.971+83_971+84del
ENST00000680018.1:c.2626+83_2626+84del	ENSP00000505347.1:n.2626+83_2626+84del
ENST00000680422.1:c.4268+83_4268+84del
ENST00000680425.1:c.2348+83_2348+84del	ENSP00000506459.1:n.2348+83_2348+84del
ENST00000680453.1:c.2638+83_2638+84del
ENST00000680790.1:c.6926+83_6926+84del	ENSP00000505335.1:n.6926+83_6926+84del
ENST00000681136.1:n.3165+83_3165+84del
ENST00000681696.1:c.2864+83_2864+84del	ENSP00000505871.1:n.2864+83_2864+84del
ENST00000681773.1:n.388+83_388+84del
ENST00000298910.11:c.7181+83_7181+84del	ENSP00000298910.7:n.7181+83_7181+84del
ENST00000430804.5:c.4477+83_4477+84del
ENST00000479187.5:n.3862+83_3862+84del
NM_198578.3:c.7181+83_7181+84del	NP_940980.3:n.7181+83_7181+84del
XM_005268629.2:c.7181+83_7181+84del	XP_005268686.1:n.7181+83_7181+84del
XM_011537877.1:c.7181+83_7181+84del	XP_011536179.1:n.7181+83_7181+84del
XM_011537879.1:c.5978+83_5978+84del	XP_011536181.1:n.5978+83_5978+84del
XR_944868.1:n.485-8810_485-8809del
XM_005268629.4:c.7181+83_7181+84del	XP_005268686.1:n.7181+83_7181+84del
XM_011537877.3:c.7181+83_7181+84del	XP_011536179.1:n.7181+83_7181+84del
XM_017018787.1:c.4097+83_4097+84del	XP_016874276.1:n.4097+83_4097+84del
XM_017018788.2:c.3443+83_3443+84del	XP_016874277.1:n.3443+83_3443+84del
XM_024448833.1:c.5978+83_5978+84del	XP_024304601.1:n.5978+83_5978+84del
XR_944868.2:n.485-8810_485-8809del
NM_198578.4:c.7181+83_7181+84del MANE Select	NP_940980.4:n.7181+83_7181+84del