Canonical Allele Identifier: CA15689302
Gene: SORL1 HGNC NCBI

Linked Data

dbSNP Id: rs2298814

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.121554173G>A , CM000673.2:g.121554173G>A GRCh38
NC_000011.9:g.121424882G>A , CM000673.1:g.121424882G>A GRCh37
NC_000011.8:g.120930092G>A NCBI36
NG_023313.1:g.106922G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000260197.12:c.2439+64G>A MANE Select ENSP00000260197.6:n.2439+64G>A
ENST00000260197.11:c.2439+64G>A ENSP00000260197.6:n.2439+64G>A
NM_003105.5:c.2439+64G>A NP_003096.1:n.2439+64G>A
XM_011542963.1:c.2439+64G>A XP_011541265.1:n.2439+64G>A
XM_011542964.1:c.2439+64G>A XP_011541266.1:n.2439+64G>A
XM_011542965.1:c.900+64G>A XP_011541267.1:n.900+64G>A
XM_011542963.3:c.2439+64G>A XP_011541265.1:n.2439+64G>A
XM_011542965.3:c.900+64G>A XP_011541267.1:n.900+64G>A
XM_017018169.2:c.2127+64G>A XP_016873658.1:n.2127+64G>A
XM_017018170.2:c.1914+64G>A XP_016873659.1:n.1914+64G>A
XM_017018171.1:c.2439+64G>A XP_016873660.1:n.2439+64G>A
XM_017018172.2:c.-110+64G>A XP_016873661.1:n.-110+64G>A
NM_003105.6:c.2439+64G>A MANE Select NP_003096.2:n.2439+64G>A