Canonical Allele Identifier: CA604503068

Gene: LRRK2

Linked Data

• dbSNP Id: rs1491226697
• gnomAD v2: 12-40692640-ATT-A
• gnomAD v3: 12-40298838-ATT-A
• gnomAD v4: 12-40298838-ATT-A
• MyVariant Identifiers: chr12:g.40692641_40692642del (hg19) ; chr12:g.40692642_40692646delinsATT (hg19) ; chr12:g.40298839_40298840del (hg38) ; chr12:g.40298840_40298844delinsATT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40298840_40298841del , CM000674.2:g.40298840_40298841del	GRCh38
NC_000012.11:g.40692642_40692643del , CM000674.1:g.40692642_40692643del	GRCh37
NC_000012.10:g.38978909_38978910del	NCBI36
NG_011709.1:g.78830_78831del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.3348-269_3348-268del MANE Select	ENSP00000298910.7:n.3348-269_3348-268del
ENST00000679360.1:c.*2257-269_*2257-268del	ENSP00000505368.1:n.*2257-269_*2257-268del
ENST00000680790.1:c.3093-269_3093-268del	ENSP00000505335.1:n.3093-269_3093-268del
ENST00000298910.11:c.3348-269_3348-268del	ENSP00000298910.7:n.3348-269_3348-268del
ENST00000343742.6:c.3348-269_3348-268del	ENSP00000341930.2:n.3348-269_3348-268del
ENST00000430804.5:c.392-269_392-268del
ENST00000479187.5:n.29-269_29-268del
NM_198578.3:c.3348-269_3348-268del	NP_940980.3:n.3348-269_3348-268del
XM_005268629.2:c.3348-269_3348-268del	XP_005268686.1:n.3348-269_3348-268del
XM_011537877.1:c.3348-269_3348-268del	XP_011536179.1:n.3348-269_3348-268del
XM_011537878.1:c.3348-269_3348-268del	XP_011536180.1:n.3348-269_3348-268del
XM_011537879.1:c.2145-269_2145-268del	XP_011536181.1:n.2145-269_2145-268del
XM_011537880.1:c.3348-269_3348-268del	XP_011536182.1:n.3348-269_3348-268del
XM_011537881.1:c.3348-269_3348-268del	XP_011536183.1:n.3348-269_3348-268del
XM_011537882.1:c.3348-269_3348-268del	XP_011536184.1:n.3348-269_3348-268del
XM_005268629.4:c.3348-269_3348-268del	XP_005268686.1:n.3348-269_3348-268del
XM_011537877.3:c.3348-269_3348-268del	XP_011536179.1:n.3348-269_3348-268del
XM_011537881.3:c.3348-269_3348-268del	XP_011536183.1:n.3348-269_3348-268del
XM_011537882.3:c.3348-269_3348-268del	XP_011536184.1:n.3348-269_3348-268del
XM_017018786.2:c.3348-269_3348-268del	XP_016874275.1:n.3348-269_3348-268del
XM_017018787.1:c.264-269_264-268del	XP_016874276.1:n.264-269_264-268del
XM_017018789.2:c.3348-269_3348-268del	XP_016874278.1:n.3348-269_3348-268del
XM_024448833.1:c.2145-269_2145-268del	XP_024304601.1:n.2145-269_2145-268del
XR_001748574.2:n.3590-269_3590-268del
NM_198578.4:c.3348-269_3348-268del MANE Select	NP_940980.4:n.3348-269_3348-268del