Canonical Allele Identifier: CA384413487

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40757312A>C (hg19) ; chr12:g.40363510A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40363510A>C , CM000674.2:g.40363510A>C	GRCh38
NC_000012.11:g.40757312A>C , CM000674.1:g.40757312A>C	GRCh37
NC_000012.10:g.39043579A>C	NCBI36
NG_011709.1:g.143500A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.7137A>C MANE Select	ENSP00000298910.7:p.Lys2379Asn
ENST00000636518.1:c.934A>C
ENST00000679360.1:c.*6046A>C	ENSP00000505368.1:n.*6046A>C
ENST00000679532.1:c.2911A>C
ENST00000679683.1:c.927A>C
ENST00000680018.1:c.2582A>C	ENSP00000505347.1:n.2582A>C
ENST00000680422.1:c.4224A>C
ENST00000680425.1:c.2304A>C	ENSP00000506459.1:n.2304A>C
ENST00000680453.1:c.2594A>C
ENST00000680790.1:c.6882A>C	ENSP00000505335.1:p.Lys2294Asn
ENST00000681136.1:n.3121A>C
ENST00000681696.1:c.2820A>C	ENSP00000505871.1:p.Lys940Asn
ENST00000681773.1:n.344A>C
ENST00000298910.11:c.7137A>C	ENSP00000298910.7:p.Lys2379Asn
ENST00000430804.5:c.4433A>C
ENST00000479187.5:n.3818A>C
NM_198578.3:c.7137A>C	NP_940980.3:p.Lys2379Asn
XM_005268629.2:c.7137A>C	XP_005268686.1:p.Lys2379Asn
XM_011537877.1:c.7137A>C	XP_011536179.1:p.Lys2379Asn
XM_011537879.1:c.5934A>C	XP_011536181.1:p.Lys1978Asn
XR_944868.1:n.485-8683T>G
XM_005268629.4:c.7137A>C	XP_005268686.1:p.Lys2379Asn
XM_011537877.3:c.7137A>C	XP_011536179.1:p.Lys2379Asn
XM_017018787.1:c.4053A>C	XP_016874276.1:p.Lys1351Asn
XM_017018788.2:c.3399A>C	XP_016874277.1:p.Lys1133Asn
XM_024448833.1:c.5934A>C	XP_024304601.1:p.Lys1978Asn
XR_944868.2:n.485-8683T>G
NM_198578.4:c.7137A>C MANE Select	NP_940980.4:p.Lys2379Asn