Canonical Allele Identifier: CA2618282097

Gene: LRRK2

Linked Data

• gnomAD v4: 12-40298458-TGTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40298461_40298463del , CM000674.2:g.40298461_40298463del	GRCh38
NC_000012.11:g.40692263_40692265del , CM000674.1:g.40692263_40692265del	GRCh37
NC_000012.10:g.38978530_38978532del	NCBI36
NG_011709.1:g.78451_78453del

Transcript Alleles

HGVS	Amino-acid change
ENST00000298910.12:c.3315_3317del MANE Select	ENSP00000298910.7:p.Val1106del
ENST00000679360.1:c.*2224_*2226del	ENSP00000505368.1:n.*2224_*2226del
ENST00000680790.1:c.3060_3062del	ENSP00000505335.1:p.Val1021del
ENST00000298910.11:c.3315_3317del	ENSP00000298910.7:p.Val1106del
ENST00000343742.6:c.3315_3317del	ENSP00000341930.2:p.Val1106del
ENST00000430804.5:c.359_361del
NM_198578.3:c.3315_3317del	NP_940980.3:p.Val1106del
XM_005268629.2:c.3315_3317del	XP_005268686.1:p.Val1106del
XM_011537877.1:c.3315_3317del	XP_011536179.1:p.Val1106del
XM_011537878.1:c.3315_3317del	XP_011536180.1:p.Val1106del
XM_011537879.1:c.2112_2114del	XP_011536181.1:p.Val705del
XM_011537880.1:c.3315_3317del	XP_011536182.1:p.Val1106del
XM_011537881.1:c.3315_3317del	XP_011536183.1:p.Val1106del
XM_011537882.1:c.3315_3317del	XP_011536184.1:p.Val1106del
XM_005268629.4:c.3315_3317del	XP_005268686.1:p.Val1106del
XM_011537877.3:c.3315_3317del	XP_011536179.1:p.Val1106del
XM_011537881.3:c.3315_3317del	XP_011536183.1:p.Val1106del
XM_011537882.3:c.3315_3317del	XP_011536184.1:p.Val1106del
XM_017018786.2:c.3315_3317del	XP_016874275.1:p.Val1106del
XM_017018787.1:c.231_233del	XP_016874276.1:p.Val78del
XM_017018789.2:c.3315_3317del	XP_016874278.1:p.Val1106del
XM_024448833.1:c.2112_2114del	XP_024304601.1:p.Val705del
XR_001748574.2:n.3557_3559del
NM_198578.4:c.3315_3317del MANE Select	NP_940980.4:p.Val1106del