Canonical Allele Identifier: CA2004951386
Gene: SORL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.121586261G= , CM000673.2:g.121586261G= GRCh38
NC_000011.9:g.121456970G= , CM000673.1:g.121456970G= GRCh37
NC_000011.8:g.120962180G= NCBI36
NG_023313.1:g.139010G=

Transcript Alleles

HGVS Amino-acid change
ENST00000260197.12:c.3746G= MANE Select ENSP00000260197.6:p.Cys1249=
ENST00000260197.11:c.3746G= ENSP00000260197.6:p.Cys1249=
ENST00000525532.5:c.578G= ENSP00000434634.1:p.Cys193=
ENST00000532694.5:c.284G= ENSP00000432131.1:p.Cys95=
ENST00000534286.5:c.476G= ENSP00000436447.1:p.Cys159=
NM_003105.5:c.3746G= NP_003096.1:p.Cys1249=
XM_011542963.1:c.3632G= XP_011541265.1:p.Cys1211=
XM_011542964.1:c.3746G= XP_011541266.1:p.Cys1249=
XM_011542965.1:c.2207G= XP_011541267.1:p.Cys736=
XM_011542966.1:c.1106G= XP_011541268.1:p.Cys369=
XM_011542967.1:c.578G= XP_011541269.1:p.Cys193=
XM_011542963.3:c.3632G= XP_011541265.1:p.Cys1211=
XM_011542965.3:c.2207G= XP_011541267.1:p.Cys736=
XM_011542967.3:c.578G= XP_011541269.1:p.Cys193=
XM_017018169.2:c.3434G= XP_016873658.1:p.Cys1145=
XM_017018170.2:c.3221G= XP_016873659.1:p.Cys1074=
XM_017018171.1:c.3746G= XP_016873660.1:p.Cys1249=
XM_017018172.2:c.1106G= XP_016873661.1:p.Cys369=
NM_003105.6:c.3746G= MANE Select NP_003096.2:p.Cys1249=