Canonical Allele Identifier: CA2004910698
Gene: SORL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.121522971T= , CM000673.2:g.121522971T= GRCh38
NC_000011.9:g.121393680T= , CM000673.1:g.121393680T= GRCh37
NC_000011.8:g.120898890T= NCBI36
NG_023313.1:g.75720T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260197.12:c.1578T= MANE Select ENSP00000260197.6:p.Ala526=
ENST00000260197.11:c.1578T= ENSP00000260197.6:p.Ala526=
ENST00000532451.1:n.1530T=
NM_003105.5:c.1578T= NP_003096.1:p.Ala526=
XM_011542963.1:c.1578T= XP_011541265.1:p.Ala526=
XM_011542964.1:c.1578T= XP_011541266.1:p.Ala526=
XM_011542965.1:c.-45T= XP_011541267.1:n.-45T=
XM_011542963.3:c.1578T= XP_011541265.1:p.Ala526=
XM_011542965.3:c.-45T= XP_011541267.1:n.-45T=
XM_017018169.2:c.1266T= XP_016873658.1:p.Ala422=
XM_017018170.2:c.1053T= XP_016873659.1:p.Ala351=
XM_017018171.1:c.1578T= XP_016873660.1:p.Ala526=
NM_003105.6:c.1578T= MANE Select NP_003096.2:p.Ala526=