Canonical Allele Identifier: CA604810567

Gene: LRRK2

Linked Data

• dbSNP Id: rs1253855401
• gnomAD v2: 12-40745299-TAACTC-T
• gnomAD v3: 12-40351497-TAACTC-T
• gnomAD v4: 12-40351497-TAACTC-T
• MyVariant Identifiers: chr12:g.40745300_40745304del (hg19) ; chr12:g.40351498_40351502del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40351498_40351502del , CM000674.2:g.40351498_40351502del	GRCh38
NC_000012.11:g.40745300_40745304del , CM000674.1:g.40745300_40745304del	GRCh37
NC_000012.10:g.39031567_39031571del	NCBI36
NG_011709.1:g.131488_131492del

Transcript Alleles

HGVS	Amino-acid change
ENST00000298910.12:c.6382-41_6382-37del MANE Select	ENSP00000298910.7:n.6382-41_6382-37del
ENST00000636518.1:c.179-41_179-37del
ENST00000679360.1:c.*5291-41_*5291-37del	ENSP00000505368.1:n.*5291-41_*5291-37del
ENST00000679532.1:c.2156-41_2156-37del
ENST00000679683.1:c.172-41_172-37del
ENST00000680018.1:c.1827-41_1827-37del	ENSP00000505347.1:n.1827-41_1827-37del
ENST00000680422.1:c.2027-41_2027-37del
ENST00000680425.1:c.1549-41_1549-37del	ENSP00000506459.1:n.1549-41_1549-37del
ENST00000680453.1:c.1839-41_1839-37del
ENST00000680790.1:c.6127-41_6127-37del	ENSP00000505335.1:n.6127-41_6127-37del
ENST00000681136.1:n.2366-41_2366-37del
ENST00000681696.1:c.2065-41_2065-37del	ENSP00000505871.1:n.2065-41_2065-37del
ENST00000298910.11:c.6382-41_6382-37del	ENSP00000298910.7:n.6382-41_6382-37del
ENST00000430804.5:c.3678-41_3678-37del
ENST00000479187.5:n.3063-41_3063-37del
NM_198578.3:c.6382-41_6382-37del	NP_940980.3:n.6382-41_6382-37del
XM_005268629.2:c.6382-41_6382-37del	XP_005268686.1:n.6382-41_6382-37del
XM_011537877.1:c.6382-41_6382-37del	XP_011536179.1:n.6382-41_6382-37del
XM_011537878.1:c.6382-41_6382-37del	XP_011536180.1:n.6382-41_6382-37del
XM_011537879.1:c.5179-41_5179-37del	XP_011536181.1:n.5179-41_5179-37del
XM_005268629.4:c.6382-41_6382-37del	XP_005268686.1:n.6382-41_6382-37del
XM_011537877.3:c.6382-41_6382-37del	XP_011536179.1:n.6382-41_6382-37del
XM_017018787.1:c.3298-41_3298-37del	XP_016874276.1:n.3298-41_3298-37del
XM_017018788.2:c.2644-41_2644-37del	XP_016874277.1:n.2644-41_2644-37del
XM_024448833.1:c.5179-41_5179-37del	XP_024304601.1:n.5179-41_5179-37del
NM_198578.4:c.6382-41_6382-37del MANE Select	NP_940980.4:n.6382-41_6382-37del