Canonical Allele Identifier: CA384403688

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40734142A>T (hg19) ; chr12:g.40340340A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40340340A>T , CM000674.2:g.40340340A>T	GRCh38
NC_000012.11:g.40734142A>T , CM000674.1:g.40734142A>T	GRCh37
NC_000012.10:g.39020409A>T	NCBI36
NG_011709.1:g.120330A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.5995A>T MANE Select	ENSP00000298910.7:p.Asn1999Tyr
ENST00000679360.1:c.*4904A>T	ENSP00000505368.1:n.*4904A>T
ENST00000679532.1:c.1769A>T
ENST00000680018.1:c.1440A>T	ENSP00000505347.1:n.1440A>T
ENST00000680422.1:c.1640A>T
ENST00000680425.1:c.1162A>T	ENSP00000506459.1:n.1162A>T
ENST00000680453.1:c.1452A>T
ENST00000680790.1:c.5740A>T	ENSP00000505335.1:p.Asn1914Tyr
ENST00000681136.1:n.1979A>T
ENST00000681696.1:c.1678A>T	ENSP00000505871.1:p.Asn560Tyr
ENST00000298910.11:c.5995A>T	ENSP00000298910.7:p.Asn1999Tyr
ENST00000430804.5:c.3291A>T
ENST00000479187.5:n.2676A>T
NM_198578.3:c.5995A>T	NP_940980.3:p.Asn1999Tyr
XM_005268629.2:c.5995A>T	XP_005268686.1:p.Asn1999Tyr
XM_011537877.1:c.5995A>T	XP_011536179.1:p.Asn1999Tyr
XM_011537878.1:c.5995A>T	XP_011536180.1:p.Asn1999Tyr
XM_011537879.1:c.4792A>T	XP_011536181.1:p.Asn1598Tyr
XM_005268629.4:c.5995A>T	XP_005268686.1:p.Asn1999Tyr
XM_011537877.3:c.5995A>T	XP_011536179.1:p.Asn1999Tyr
XM_017018787.1:c.2911A>T	XP_016874276.1:p.Asn971Tyr
XM_017018788.2:c.2257A>T	XP_016874277.1:p.Asn753Tyr
XM_024448833.1:c.4792A>T	XP_024304601.1:p.Asn1598Tyr
NM_198578.4:c.5995A>T MANE Select	NP_940980.4:p.Asn1999Tyr