Canonical Allele Identifier: CA2004883295
Gene: SORL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.121486225_121486228delinsCCTG , CM000673.2:g.121486225_121486228delinsCCTG GRCh38
NC_000011.9:g.121356934_121356937delinsCCTG , CM000673.1:g.121356934_121356937delinsCCTG GRCh37
NC_000011.8:g.120862144_120862147delinsCCTG NCBI36
NG_023313.1:g.38974_38977delinsCCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000260197.12:c.529-1807_529-1804delinsCCTG MANE Select ENSP00000260197.6:n.529-1807_529-1804delinsCCTG
ENST00000260197.11:c.529-1807_529-1804delinsCCTG ENSP00000260197.6:n.529-1807_529-1804delinsCCTG
ENST00000532451.1:n.481-1807_481-1804delinsCCTG
NM_003105.5:c.529-1807_529-1804delinsCCTG NP_003096.1:n.529-1807_529-1804delinsCCTG
XM_011542963.1:c.529-1807_529-1804delinsCCTG XP_011541265.1:n.529-1807_529-1804delinsCCTG
XM_011542964.1:c.529-1807_529-1804delinsCCTG XP_011541266.1:n.529-1807_529-1804delinsCCTG
XM_011542963.3:c.529-1807_529-1804delinsCCTG XP_011541265.1:n.529-1807_529-1804delinsCCTG
XM_017018169.2:c.217-1807_217-1804delinsCCTG XP_016873658.1:n.217-1807_217-1804delinsCCTG
XM_017018171.1:c.529-1807_529-1804delinsCCTG XP_016873660.1:n.529-1807_529-1804delinsCCTG
NM_003105.6:c.529-1807_529-1804delinsCCTG MANE Select NP_003096.2:n.529-1807_529-1804delinsCCTG