Canonical Allele Identifier: CA477218629

Gene: SORL1

Linked Data

• MyVariant Identifiers: chr11:g.121424692C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.121553983C>G , CM000673.2:g.121553983C>G	GRCh38
NC_000011.9:g.121424692C>G , CM000673.1:g.121424692C>G	GRCh37
NC_000011.8:g.120929902C>G	NCBI36
NG_023313.1:g.106732C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000260197.12:c.2313C>G MANE Select	ENSP00000260197.6:p.Arg771=
ENST00000260197.11:c.2313C>G	ENSP00000260197.6:p.Arg771=
NM_003105.5:c.2313C>G	NP_003096.1:p.Arg771=
XM_011542963.1:c.2313C>G	XP_011541265.1:p.Arg771=
XM_011542964.1:c.2313C>G	XP_011541266.1:p.Arg771=
XM_011542965.1:c.774C>G	XP_011541267.1:p.Arg258=
XM_011542963.3:c.2313C>G	XP_011541265.1:p.Arg771=
XM_011542965.3:c.774C>G	XP_011541267.1:p.Arg258=
XM_017018169.2:c.2001C>G	XP_016873658.1:p.Arg667=
XM_017018170.2:c.1788C>G	XP_016873659.1:p.Arg596=
XM_017018171.1:c.2313C>G	XP_016873660.1:p.Arg771=
XM_017018172.2:c.-236C>G	XP_016873661.1:n.-236C>G
NM_003105.6:c.2313C>G MANE Select	NP_003096.2:p.Arg771=