Canonical Allele Identifier: CA2004951384
Gene: SORL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.121586254G= , CM000673.2:g.121586254G= GRCh38
NC_000011.9:g.121456963G= , CM000673.1:g.121456963G= GRCh37
NC_000011.8:g.120962173G= NCBI36
NG_023313.1:g.139003G=

Transcript Alleles

HGVS Amino-acid change
ENST00000260197.12:c.3739G= MANE Select ENSP00000260197.6:p.Gly1247=
ENST00000260197.11:c.3739G= ENSP00000260197.6:p.Gly1247=
ENST00000525532.5:c.571G= ENSP00000434634.1:p.Gly191=
ENST00000532694.5:c.277G= ENSP00000432131.1:p.Gly93=
ENST00000534286.5:c.469G= ENSP00000436447.1:p.Gly157=
NM_003105.5:c.3739G= NP_003096.1:p.Gly1247=
XM_011542963.1:c.3625G= XP_011541265.1:p.Gly1209=
XM_011542964.1:c.3739G= XP_011541266.1:p.Gly1247=
XM_011542965.1:c.2200G= XP_011541267.1:p.Gly734=
XM_011542966.1:c.1099G= XP_011541268.1:p.Gly367=
XM_011542967.1:c.571G= XP_011541269.1:p.Gly191=
XM_011542963.3:c.3625G= XP_011541265.1:p.Gly1209=
XM_011542965.3:c.2200G= XP_011541267.1:p.Gly734=
XM_011542967.3:c.571G= XP_011541269.1:p.Gly191=
XM_017018169.2:c.3427G= XP_016873658.1:p.Gly1143=
XM_017018170.2:c.3214G= XP_016873659.1:p.Gly1072=
XM_017018171.1:c.3739G= XP_016873660.1:p.Gly1247=
XM_017018172.2:c.1099G= XP_016873661.1:p.Gly367=
NM_003105.6:c.3739G= MANE Select NP_003096.2:p.Gly1247=