Canonical Allele Identifier: CA384413179

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40757232A>T (hg19) ; chr12:g.40363430A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40363430A>T , CM000674.2:g.40363430A>T	GRCh38
NC_000012.11:g.40757232A>T , CM000674.1:g.40757232A>T	GRCh37
NC_000012.10:g.39043499A>T	NCBI36
NG_011709.1:g.143420A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000298910.12:c.7057A>T MANE Select	ENSP00000298910.7:p.Asn2353Tyr
ENST00000636518.1:c.854A>T
ENST00000679360.1:c.*5966A>T	ENSP00000505368.1:n.*5966A>T
ENST00000679532.1:c.2831A>T
ENST00000679683.1:c.847A>T
ENST00000680018.1:c.2502A>T	ENSP00000505347.1:n.2502A>T
ENST00000680422.1:c.4144A>T
ENST00000680425.1:c.2224A>T	ENSP00000506459.1:n.2224A>T
ENST00000680453.1:c.2514A>T
ENST00000680790.1:c.6802A>T	ENSP00000505335.1:p.Asn2268Tyr
ENST00000681136.1:n.3041A>T
ENST00000681696.1:c.2740A>T	ENSP00000505871.1:p.Asn914Tyr
ENST00000681773.1:n.264A>T
ENST00000298910.11:c.7057A>T	ENSP00000298910.7:p.Asn2353Tyr
ENST00000430804.5:c.4353A>T
ENST00000479187.5:n.3738A>T
NM_198578.3:c.7057A>T	NP_940980.3:p.Asn2353Tyr
XM_005268629.2:c.7057A>T	XP_005268686.1:p.Asn2353Tyr
XM_011537877.1:c.7057A>T	XP_011536179.1:p.Asn2353Tyr
XM_011537879.1:c.5854A>T	XP_011536181.1:p.Asn1952Tyr
XR_944868.1:n.485-8603T>A
XM_005268629.4:c.7057A>T	XP_005268686.1:p.Asn2353Tyr
XM_011537877.3:c.7057A>T	XP_011536179.1:p.Asn2353Tyr
XM_017018787.1:c.3973A>T	XP_016874276.1:p.Asn1325Tyr
XM_017018788.2:c.3319A>T	XP_016874277.1:p.Asn1107Tyr
XM_024448833.1:c.5854A>T	XP_024304601.1:p.Asn1952Tyr
XR_944868.2:n.485-8603T>A
NM_198578.4:c.7057A>T MANE Select	NP_940980.4:p.Asn2353Tyr