Canonical Allele Identifier: CA2004947511
Gene: SORL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.121577370A= , CM000673.2:g.121577370A= GRCh38
NC_000011.9:g.121448079A= , CM000673.1:g.121448079A= GRCh37
NC_000011.8:g.120953289A= NCBI36
NG_023313.1:g.130119A=

Transcript Alleles

HGVS Amino-acid change
ENST00000260197.12:c.3550A= MANE Select ENSP00000260197.6:p.Arg1184=
ENST00000260197.11:c.3550A= ENSP00000260197.6:p.Arg1184=
ENST00000525532.5:c.382A= ENSP00000434634.1:p.Arg128=
ENST00000532694.5:c.88A= ENSP00000432131.1:p.Arg30=
ENST00000534286.5:c.280A= ENSP00000436447.1:p.Arg94=
NM_003105.5:c.3550A= NP_003096.1:p.Arg1184=
XM_011542963.1:c.3436A= XP_011541265.1:p.Arg1146=
XM_011542964.1:c.3550A= XP_011541266.1:p.Arg1184=
XM_011542965.1:c.2011A= XP_011541267.1:p.Arg671=
XM_011542966.1:c.910A= XP_011541268.1:p.Arg304=
XM_011542967.1:c.382A= XP_011541269.1:p.Arg128=
XM_011542963.3:c.3436A= XP_011541265.1:p.Arg1146=
XM_011542965.3:c.2011A= XP_011541267.1:p.Arg671=
XM_011542967.3:c.382A= XP_011541269.1:p.Arg128=
XM_017018169.2:c.3238A= XP_016873658.1:p.Arg1080=
XM_017018170.2:c.3025A= XP_016873659.1:p.Arg1009=
XM_017018171.1:c.3550A= XP_016873660.1:p.Arg1184=
XM_017018172.2:c.910A= XP_016873661.1:p.Arg304=
NM_003105.6:c.3550A= MANE Select NP_003096.2:p.Arg1184=