Canonical Allele Identifier: CA2004910225
Gene: SORL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.121522368T= , CM000673.2:g.121522368T= GRCh38
NC_000011.9:g.121393077T= , CM000673.1:g.121393077T= GRCh37
NC_000011.8:g.120898287T= NCBI36
NG_023313.1:g.75117T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260197.12:c.1405-218T= MANE Select ENSP00000260197.6:n.1405-218T=
ENST00000260197.11:c.1405-218T= ENSP00000260197.6:n.1405-218T=
ENST00000532451.1:n.1357-218T=
NM_003105.5:c.1405-218T= NP_003096.1:n.1405-218T=
XM_011542963.1:c.1405-218T= XP_011541265.1:n.1405-218T=
XM_011542964.1:c.1405-218T= XP_011541266.1:n.1405-218T=
XM_011542965.1:c.-218-218T= XP_011541267.1:n.-218-218T=
XM_011542963.3:c.1405-218T= XP_011541265.1:n.1405-218T=
XM_011542965.3:c.-218-218T= XP_011541267.1:n.-218-218T=
XM_017018169.2:c.1093-218T= XP_016873658.1:n.1093-218T=
XM_017018170.2:c.880-218T= XP_016873659.1:n.880-218T=
XM_017018171.1:c.1405-218T= XP_016873660.1:n.1405-218T=
NM_003105.6:c.1405-218T= MANE Select NP_003096.2:n.1405-218T=