Canonical Allele Identifier: CA2004919360

Gene: SORL1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.121558769T= , CM000673.2:g.121558769T=	GRCh38
NC_000011.9:g.121429478T= , CM000673.1:g.121429478T=	GRCh37
NC_000011.8:g.120934688T=	NCBI36
NG_023313.1:g.111518T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000260197.12:c.2842T= MANE Select	ENSP00000260197.6:p.Phe948=
ENST00000260197.11:c.2842T=	ENSP00000260197.6:p.Phe948=
ENST00000524873.1:n.570T=
ENST00000529445.1:n.548T=
NM_003105.5:c.2842T=	NP_003096.1:p.Phe948=
XM_011542963.1:c.2842T=	XP_011541265.1:p.Phe948=
XM_011542964.1:c.2842T=	XP_011541266.1:p.Phe948=
XM_011542965.1:c.1303T=	XP_011541267.1:p.Phe435=
XM_011542966.1:c.202T=	XP_011541268.1:p.Phe68=
XM_011542963.3:c.2842T=	XP_011541265.1:p.Phe948=
XM_011542965.3:c.1303T=	XP_011541267.1:p.Phe435=
XM_017018169.2:c.2530T=	XP_016873658.1:p.Phe844=
XM_017018170.2:c.2317T=	XP_016873659.1:p.Phe773=
XM_017018171.1:c.2842T=	XP_016873660.1:p.Phe948=
XM_017018172.2:c.202T=	XP_016873661.1:p.Phe68=
NM_003105.6:c.2842T= MANE Select	NP_003096.2:p.Phe948=