Canonical Allele Identifier: CA2004919317

Gene: SORL1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.121558669C= , CM000673.2:g.121558669C=	GRCh38
NC_000011.9:g.121429378C= , CM000673.1:g.121429378C=	GRCh37
NC_000011.8:g.120934588C=	NCBI36
NG_023313.1:g.111418C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000260197.12:c.2742C= MANE Select	ENSP00000260197.6:p.His914=
ENST00000260197.11:c.2742C=	ENSP00000260197.6:p.His914=
ENST00000524873.1:n.470C=
ENST00000529445.1:n.448C=
NM_003105.5:c.2742C=	NP_003096.1:p.His914=
XM_011542963.1:c.2742C=	XP_011541265.1:p.His914=
XM_011542964.1:c.2742C=	XP_011541266.1:p.His914=
XM_011542965.1:c.1203C=	XP_011541267.1:p.His401=
XM_011542966.1:c.102C=	XP_011541268.1:p.His34=
XM_011542963.3:c.2742C=	XP_011541265.1:p.His914=
XM_011542965.3:c.1203C=	XP_011541267.1:p.His401=
XM_017018169.2:c.2430C=	XP_016873658.1:p.His810=
XM_017018170.2:c.2217C=	XP_016873659.1:p.His739=
XM_017018171.1:c.2742C=	XP_016873660.1:p.His914=
XM_017018172.2:c.102C=	XP_016873661.1:p.His34=
NM_003105.6:c.2742C= MANE Select	NP_003096.2:p.His914=