Canonical Allele Identifier: CA384413185

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40757233A>G (hg19) ; chr12:g.40363431A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40363431A>G , CM000674.2:g.40363431A>G	GRCh38
NC_000012.11:g.40757233A>G , CM000674.1:g.40757233A>G	GRCh37
NC_000012.10:g.39043500A>G	NCBI36
NG_011709.1:g.143421A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000298910.12:c.7058A>G MANE Select	ENSP00000298910.7:p.Asn2353Ser
ENST00000636518.1:c.855A>G
ENST00000679360.1:c.*5967A>G	ENSP00000505368.1:n.*5967A>G
ENST00000679532.1:c.2832A>G
ENST00000679683.1:c.848A>G
ENST00000680018.1:c.2503A>G	ENSP00000505347.1:n.2503A>G
ENST00000680422.1:c.4145A>G
ENST00000680425.1:c.2225A>G	ENSP00000506459.1:n.2225A>G
ENST00000680453.1:c.2515A>G
ENST00000680790.1:c.6803A>G	ENSP00000505335.1:p.Asn2268Ser
ENST00000681136.1:n.3042A>G
ENST00000681696.1:c.2741A>G	ENSP00000505871.1:p.Asn914Ser
ENST00000681773.1:n.265A>G
ENST00000298910.11:c.7058A>G	ENSP00000298910.7:p.Asn2353Ser
ENST00000430804.5:c.4354A>G
ENST00000479187.5:n.3739A>G
NM_198578.3:c.7058A>G	NP_940980.3:p.Asn2353Ser
XM_005268629.2:c.7058A>G	XP_005268686.1:p.Asn2353Ser
XM_011537877.1:c.7058A>G	XP_011536179.1:p.Asn2353Ser
XM_011537879.1:c.5855A>G	XP_011536181.1:p.Asn1952Ser
XR_944868.1:n.485-8604T>C
XM_005268629.4:c.7058A>G	XP_005268686.1:p.Asn2353Ser
XM_011537877.3:c.7058A>G	XP_011536179.1:p.Asn2353Ser
XM_017018787.1:c.3974A>G	XP_016874276.1:p.Asn1325Ser
XM_017018788.2:c.3320A>G	XP_016874277.1:p.Asn1107Ser
XM_024448833.1:c.5855A>G	XP_024304601.1:p.Asn1952Ser
XR_944868.2:n.485-8604T>C
NM_198578.4:c.7058A>G MANE Select	NP_940980.4:p.Asn2353Ser