Canonical Allele Identifier: CA2200318058

Gene: LRRK1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.101018357G= , CM000677.2:g.101018357G=	GRCh38
NC_000015.9:g.101558562G= , CM000677.1:g.101558562G=	GRCh37
NC_000015.8:g.99376085G=	NCBI36
NG_052791.1:g.104341G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388948.8:c.1610-2696G= MANE Select	ENSP00000373600.3:n.1610-2696G=
ENST00000388948.7:c.1610-2696G=	ENSP00000373600.3:n.1610-2696G=
ENST00000525284.5:c.1610-2696G=	ENSP00000433069.1:n.1610-2696G=
ENST00000531270.5:c.1610-2696G=	ENSP00000431668.1:n.1610-2696G=
NM_024652.4:c.1610-2696G=	NP_078928.3:n.1610-2696G=
XM_011522012.1:c.1610-2696G=	XP_011520314.1:n.1610-2696G=
XM_011522013.1:c.1610-2696G=	XP_011520315.1:n.1610-2696G=
XM_011522014.1:c.1610-2696G=	XP_011520316.1:n.1610-2696G=
XM_011522015.1:c.866-2696G=	XP_011520317.1:n.866-2696G=
XM_011522016.1:c.1307-2696G=	XP_011520318.1:n.1307-2696G=
XM_011522019.1:c.1610-2696G=	XP_011520321.1:n.1610-2696G=
XR_931905.1:n.1964-2696G=
NM_024652.5:c.1610-2696G=	NP_078928.3:n.1610-2696G=
XM_011522012.2:c.1610-2696G=	XP_011520314.1:n.1610-2696G=
XM_011522013.2:c.1610-2696G=	XP_011520315.1:n.1610-2696G=
XM_011522014.2:c.1610-2696G=	XP_011520316.1:n.1610-2696G=
XM_011522015.3:c.866-2696G=	XP_011520317.1:n.866-2696G=
XM_011522016.2:c.1307-2696G=	XP_011520318.1:n.1307-2696G=
XM_011522019.2:c.1610-2696G=	XP_011520321.1:n.1610-2696G=
XM_017022570.1:c.137-2696G=	XP_016878059.1:n.137-2696G=
XR_931905.2:n.2167-2696G=
NM_024652.6:c.1610-2696G= MANE Select	NP_078928.3:n.1610-2696G=