Canonical Allele Identifier: CA384406496

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40745356A>G (hg19) ; chr12:g.40351554A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40351554A>G , CM000674.2:g.40351554A>G	GRCh38
NC_000012.11:g.40745356A>G , CM000674.1:g.40745356A>G	GRCh37
NC_000012.10:g.39031623A>G	NCBI36
NG_011709.1:g.131544A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.6397A>G MANE Select	ENSP00000298910.7:p.Asn2133Asp
ENST00000636518.1:c.194A>G
ENST00000679360.1:c.*5306A>G	ENSP00000505368.1:n.*5306A>G
ENST00000679532.1:c.2171A>G
ENST00000679683.1:c.187A>G
ENST00000680018.1:c.1842A>G	ENSP00000505347.1:n.1842A>G
ENST00000680422.1:c.2042A>G
ENST00000680425.1:c.1564A>G	ENSP00000506459.1:n.1564A>G
ENST00000680453.1:c.1854A>G
ENST00000680790.1:c.6142A>G	ENSP00000505335.1:p.Asn2048Asp
ENST00000681136.1:n.2381A>G
ENST00000681696.1:c.2080A>G	ENSP00000505871.1:p.Asn694Asp
ENST00000298910.11:c.6397A>G	ENSP00000298910.7:p.Asn2133Asp
ENST00000430804.5:c.3693A>G
ENST00000479187.5:n.3078A>G
NM_198578.3:c.6397A>G	NP_940980.3:p.Asn2133Asp
XM_005268629.2:c.6397A>G	XP_005268686.1:p.Asn2133Asp
XM_011537877.1:c.6397A>G	XP_011536179.1:p.Asn2133Asp
XM_011537878.1:c.6397A>G	XP_011536180.1:p.Asn2133Asp
XM_011537879.1:c.5194A>G	XP_011536181.1:p.Asn1732Asp
XM_005268629.4:c.6397A>G	XP_005268686.1:p.Asn2133Asp
XM_011537877.3:c.6397A>G	XP_011536179.1:p.Asn2133Asp
XM_017018787.1:c.3313A>G	XP_016874276.1:p.Asn1105Asp
XM_017018788.2:c.2659A>G	XP_016874277.1:p.Asn887Asp
XM_024448833.1:c.5194A>G	XP_024304601.1:p.Asn1732Asp
NM_198578.4:c.6397A>G MANE Select	NP_940980.4:p.Asn2133Asp