Canonical Allele Identifier: CA2618286434

Gene: LRRK2

Linked Data

• gnomAD v4: 12-40363393-TCTCTGTAGG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40363394_40363402del , CM000674.2:g.40363394_40363402del	GRCh38
NC_000012.11:g.40757196_40757204del , CM000674.1:g.40757196_40757204del	GRCh37
NC_000012.10:g.39043463_39043471del	NCBI36
NG_011709.1:g.143384_143392del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.7029-8_7029del
ENST00000636518.1:c.826-8_826del
ENST00000679360.1:c.*5938-8_*5938del
ENST00000679532.1:c.2803-8_2803del
ENST00000679683.1:c.819-8_819del
ENST00000680018.1:c.2474-8_2474del
ENST00000680422.1:c.4116-8_4116del
ENST00000680425.1:c.2196-8_2196del
ENST00000680453.1:c.2486-8_2486del
ENST00000680790.1:c.6774-8_6774del
ENST00000681136.1:n.3013-8_3013del
ENST00000681696.1:c.2712-8_2712del
ENST00000681773.1:n.236-8_236del
ENST00000298910.11:c.7029-8_7029del
ENST00000430804.5:c.4325-8_4325del
ENST00000479187.5:n.3710-8_3710del
NM_198578.3:c.7029-8_7029del
XM_005268629.2:c.7029-8_7029del
XM_011537877.1:c.7029-8_7029del
XM_011537879.1:c.5826-8_5826del
XR_944868.1:n.485-8575_485-8567del
XM_005268629.4:c.7029-8_7029del
XM_011537877.3:c.7029-8_7029del
XM_017018787.1:c.3945-8_3945del
XM_017018788.2:c.3291-8_3291del
XM_024448833.1:c.5826-8_5826del
XR_944868.2:n.485-8575_485-8567del
NM_198578.4:c.7029-8_7029del