Canonical Allele Identifier: CA2616509335
Gene: SORL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.121631075_121631089del , CM000673.2:g.121631075_121631089del GRCh38
NC_000011.9:g.121501784_121501798del , CM000673.1:g.121501784_121501798del GRCh37
NC_000011.8:g.121006994_121007008del NCBI36
NG_023313.1:g.183824_183838del

Transcript Alleles

HGVS Amino-acid change
ENST00000260197.12:c.*1512_*1526del MANE Select ENSP00000260197.6:n.*1512_*1526del
ENST00000260197.11:c.*1512_*1526del ENSP00000260197.6:n.*1512_*1526del
ENST00000530365.1:n.759-941_759-927del
NM_003105.5:c.*1512_*1526del NP_003096.1:n.*1512_*1526del
XM_011542963.1:c.*1512_*1526del XP_011541265.1:n.*1512_*1526del
XM_011542965.1:c.*1512_*1526del XP_011541267.1:n.*1512_*1526del
XM_011542966.1:c.*1512_*1526del XP_011541268.1:n.*1512_*1526del
XM_011542967.1:c.*1512_*1526del XP_011541269.1:n.*1512_*1526del
XM_011542965.3:c.*1512_*1526del XP_011541267.1:n.*1512_*1526del
XM_011542967.3:c.*1512_*1526del XP_011541269.1:n.*1512_*1526del
XM_017018172.2:c.*1512_*1526del XP_016873661.1:n.*1512_*1526del
NM_003105.6:c.*1512_*1526del MANE Select NP_003096.2:n.*1512_*1526del