Canonical Allele Identifier: CA2004910326
Gene: SORL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.121522467_121522468delinsCT , CM000673.2:g.121522467_121522468delinsCT GRCh38
NC_000011.9:g.121393176_121393177delinsCT , CM000673.1:g.121393176_121393177delinsCT GRCh37
NC_000011.8:g.120898386_120898387delinsCT NCBI36
NG_023313.1:g.75216_75217delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000260197.12:c.1405-119_1405-118delinsCT MANE Select ENSP00000260197.6:n.1405-119_1405-118delinsCT
ENST00000260197.11:c.1405-119_1405-118delinsCT ENSP00000260197.6:n.1405-119_1405-118delinsCT
ENST00000532451.1:n.1357-119_1357-118delinsCT
NM_003105.5:c.1405-119_1405-118delinsCT NP_003096.1:n.1405-119_1405-118delinsCT
XM_011542963.1:c.1405-119_1405-118delinsCT XP_011541265.1:n.1405-119_1405-118delinsCT
XM_011542964.1:c.1405-119_1405-118delinsCT XP_011541266.1:n.1405-119_1405-118delinsCT
XM_011542965.1:c.-218-119_-218-118delinsCT XP_011541267.1:n.-218-119_-218-118delinsCT
XM_011542963.3:c.1405-119_1405-118delinsCT XP_011541265.1:n.1405-119_1405-118delinsCT
XM_011542965.3:c.-218-119_-218-118delinsCT XP_011541267.1:n.-218-119_-218-118delinsCT
XM_017018169.2:c.1093-119_1093-118delinsCT XP_016873658.1:n.1093-119_1093-118delinsCT
XM_017018170.2:c.880-119_880-118delinsCT XP_016873659.1:n.880-119_880-118delinsCT
XM_017018171.1:c.1405-119_1405-118delinsCT XP_016873660.1:n.1405-119_1405-118delinsCT
NM_003105.6:c.1405-119_1405-118delinsCT MANE Select NP_003096.2:n.1405-119_1405-118delinsCT