Canonical Allele Identifier: CA2030995348
Gene: LRRK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40320237_40320241delinsTCAAA , CM000674.2:g.40320237_40320241delinsTCAAA GRCh38
NC_000012.11:g.40714039_40714043delinsTCAAA , CM000674.1:g.40714039_40714043delinsTCAAA GRCh37
NC_000012.10:g.39000306_39000310delinsTCAAA NCBI36
NG_011709.1:g.100227_100231delinsTCAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000298910.12:c.5015+62_5015+66delinsTCAAA MANE Select ENSP00000298910.7:n.5015+62_5015+66delinsTCAAA
ENST00000679360.1:c.*3924+62_*3924+66delinsTCAAA ENSP00000505368.1:n.*3924+62_*3924+66delinsTCAAA
ENST00000679532.1:c.789+62_789+66delinsTCAAA
ENST00000680018.1:c.460+62_460+66delinsTCAAA ENSP00000505347.1:n.460+62_460+66delinsTCAAA
ENST00000680422.1:c.660+62_660+66delinsTCAAA
ENST00000680425.1:c.183-797_183-793delinsTCAAA ENSP00000506459.1:n.183-797_183-793delinsTCAAA
ENST00000680453.1:c.473-797_473-793delinsTCAAA
ENST00000680790.1:c.4760+62_4760+66delinsTCAAA ENSP00000505335.1:n.4760+62_4760+66delinsTCAAA
ENST00000681136.1:n.999+62_999+66delinsTCAAA
ENST00000681696.1:c.698+62_698+66delinsTCAAA ENSP00000505871.1:n.698+62_698+66delinsTCAAA
ENST00000298910.11:c.5015+62_5015+66delinsTCAAA ENSP00000298910.7:n.5015+62_5015+66delinsTCAAA
ENST00000430804.5:c.2311+62_2311+66delinsTCAAA
ENST00000479187.5:n.1696+62_1696+66delinsTCAAA
NM_198578.3:c.5015+62_5015+66delinsTCAAA NP_940980.3:n.5015+62_5015+66delinsTCAAA
XM_005268629.2:c.5015+62_5015+66delinsTCAAA XP_005268686.1:n.5015+62_5015+66delinsTCAAA
XM_011537877.1:c.5015+62_5015+66delinsTCAAA XP_011536179.1:n.5015+62_5015+66delinsTCAAA
XM_011537878.1:c.5015+62_5015+66delinsTCAAA XP_011536180.1:n.5015+62_5015+66delinsTCAAA
XM_011537879.1:c.3812+62_3812+66delinsTCAAA XP_011536181.1:n.3812+62_3812+66delinsTCAAA
XM_011537881.1:c.4828-797_4828-793delinsTCAAA XP_011536183.1:n.4828-797_4828-793delinsTCAAA
XM_005268629.4:c.5015+62_5015+66delinsTCAAA XP_005268686.1:n.5015+62_5015+66delinsTCAAA
XM_011537877.3:c.5015+62_5015+66delinsTCAAA XP_011536179.1:n.5015+62_5015+66delinsTCAAA
XM_011537881.3:c.4828-797_4828-793delinsTCAAA XP_011536183.1:n.4828-797_4828-793delinsTCAAA
XM_017018787.1:c.1931+62_1931+66delinsTCAAA XP_016874276.1:n.1931+62_1931+66delinsTCAAA
XM_017018788.2:c.1277+62_1277+66delinsTCAAA XP_016874277.1:n.1277+62_1277+66delinsTCAAA
XM_024448833.1:c.3812+62_3812+66delinsTCAAA XP_024304601.1:n.3812+62_3812+66delinsTCAAA
XR_001748574.2:n.5383+62_5383+66delinsTCAAA
NM_198578.4:c.5015+62_5015+66delinsTCAAA MANE Select NP_940980.4:n.5015+62_5015+66delinsTCAAA