Canonical Allele Identifier: CA2004947512
Gene: SORL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.121577372G= , CM000673.2:g.121577372G= GRCh38
NC_000011.9:g.121448081G= , CM000673.1:g.121448081G= GRCh37
NC_000011.8:g.120953291G= NCBI36
NG_023313.1:g.130121G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260197.12:c.3552G= MANE Select ENSP00000260197.6:p.Arg1184=
ENST00000260197.11:c.3552G= ENSP00000260197.6:p.Arg1184=
ENST00000525532.5:c.384G= ENSP00000434634.1:p.Arg128=
ENST00000532694.5:c.90G= ENSP00000432131.1:p.Arg30=
ENST00000534286.5:c.282G= ENSP00000436447.1:p.Arg94=
NM_003105.5:c.3552G= NP_003096.1:p.Arg1184=
XM_011542963.1:c.3438G= XP_011541265.1:p.Arg1146=
XM_011542964.1:c.3552G= XP_011541266.1:p.Arg1184=
XM_011542965.1:c.2013G= XP_011541267.1:p.Arg671=
XM_011542966.1:c.912G= XP_011541268.1:p.Arg304=
XM_011542967.1:c.384G= XP_011541269.1:p.Arg128=
XM_011542963.3:c.3438G= XP_011541265.1:p.Arg1146=
XM_011542965.3:c.2013G= XP_011541267.1:p.Arg671=
XM_011542967.3:c.384G= XP_011541269.1:p.Arg128=
XM_017018169.2:c.3240G= XP_016873658.1:p.Arg1080=
XM_017018170.2:c.3027G= XP_016873659.1:p.Arg1009=
XM_017018171.1:c.3552G= XP_016873660.1:p.Arg1184=
XM_017018172.2:c.912G= XP_016873661.1:p.Arg304=
NM_003105.6:c.3552G= MANE Select NP_003096.2:p.Arg1184=