Canonical Allele Identifier: CA2004919375

Gene: SORL1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.121558810G= , CM000673.2:g.121558810G=	GRCh38
NC_000011.9:g.121429519G= , CM000673.1:g.121429519G=	GRCh37
NC_000011.8:g.120934729G=	NCBI36
NG_023313.1:g.111559G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260197.12:c.2883G= MANE Select	ENSP00000260197.6:p.Pro961=
ENST00000260197.11:c.2883G=	ENSP00000260197.6:p.Pro961=
ENST00000529445.1:n.589G=
NM_003105.5:c.2883G=	NP_003096.1:p.Pro961=
XM_011542963.1:c.2883G=	XP_011541265.1:p.Pro961=
XM_011542964.1:c.2883G=	XP_011541266.1:p.Pro961=
XM_011542965.1:c.1344G=	XP_011541267.1:p.Pro448=
XM_011542966.1:c.243G=	XP_011541268.1:p.Pro81=
XM_011542963.3:c.2883G=	XP_011541265.1:p.Pro961=
XM_011542965.3:c.1344G=	XP_011541267.1:p.Pro448=
XM_017018169.2:c.2571G=	XP_016873658.1:p.Pro857=
XM_017018170.2:c.2358G=	XP_016873659.1:p.Pro786=
XM_017018171.1:c.2883G=	XP_016873660.1:p.Pro961=
XM_017018172.2:c.243G=	XP_016873661.1:p.Pro81=
NM_003105.6:c.2883G= MANE Select	NP_003096.2:p.Pro961=