Canonical Allele Identifier: CA604504564

Gene: LRRK2

Linked Data

• dbSNP Id: rs1285632252
• gnomAD v2: 12-40733960-CTTAACT-C
• gnomAD v3: 12-40340158-CTTAACT-C
• gnomAD v4: 12-40340158-CTTAACT-C
• MyVariant Identifiers: chr12:g.40733961_40733966del (hg19) ; chr12:g.40340159_40340164del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40340163_40340168del , CM000674.2:g.40340163_40340168del	GRCh38
NC_000012.11:g.40733965_40733970del , CM000674.1:g.40733965_40733970del	GRCh37
NC_000012.10:g.39020232_39020237del	NCBI36
NG_011709.1:g.120153_120158del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.5949-131_5949-126del MANE Select	ENSP00000298910.7:n.5949-131_5949-126del
ENST00000679360.1:c.*4858-131_*4858-126del	ENSP00000505368.1:n.*4858-131_*4858-126del
ENST00000679532.1:c.1723-131_1723-126del
ENST00000680018.1:c.1394-131_1394-126del	ENSP00000505347.1:n.1394-131_1394-126del
ENST00000680422.1:c.1594-131_1594-126del
ENST00000680425.1:c.1116-131_1116-126del	ENSP00000506459.1:n.1116-131_1116-126del
ENST00000680453.1:c.1406-131_1406-126del
ENST00000680790.1:c.5694-131_5694-126del	ENSP00000505335.1:n.5694-131_5694-126del
ENST00000681136.1:n.1933-131_1933-126del
ENST00000681696.1:c.1632-131_1632-126del	ENSP00000505871.1:n.1632-131_1632-126del
ENST00000298910.11:c.5949-131_5949-126del	ENSP00000298910.7:n.5949-131_5949-126del
ENST00000430804.5:c.3245-131_3245-126del
ENST00000479187.5:n.2630-131_2630-126del
NM_198578.3:c.5949-131_5949-126del	NP_940980.3:n.5949-131_5949-126del
XM_005268629.2:c.5949-131_5949-126del	XP_005268686.1:n.5949-131_5949-126del
XM_011537877.1:c.5949-131_5949-126del	XP_011536179.1:n.5949-131_5949-126del
XM_011537878.1:c.5949-131_5949-126del	XP_011536180.1:n.5949-131_5949-126del
XM_011537879.1:c.4746-131_4746-126del	XP_011536181.1:n.4746-131_4746-126del
XM_005268629.4:c.5949-131_5949-126del	XP_005268686.1:n.5949-131_5949-126del
XM_011537877.3:c.5949-131_5949-126del	XP_011536179.1:n.5949-131_5949-126del
XM_017018787.1:c.2865-131_2865-126del	XP_016874276.1:n.2865-131_2865-126del
XM_017018788.2:c.2211-131_2211-126del	XP_016874277.1:n.2211-131_2211-126del
XM_024448833.1:c.4746-131_4746-126del	XP_024304601.1:n.4746-131_4746-126del
NM_198578.4:c.5949-131_5949-126del MANE Select	NP_940980.4:n.5949-131_5949-126del