Canonical Allele Identifier: CA2004949472
Gene: SORL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.121581942T>G , CM000673.2:g.121581942T>G GRCh38
NC_000011.9:g.121452651T>G , CM000673.1:g.121452651T>G GRCh37
NC_000011.8:g.120957861T>G NCBI36
NG_023313.1:g.134691T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000260197.12:c.3581-1516T>G MANE Select ENSP00000260197.6:n.3581-1516T>G
ENST00000260197.11:c.3581-1516T>G ENSP00000260197.6:n.3581-1516T>G
ENST00000525532.5:c.413-1516T>G ENSP00000434634.1:n.413-1516T>G
ENST00000532694.5:c.119-1516T>G ENSP00000432131.1:n.119-1516T>G
ENST00000534286.5:c.311-1516T>G ENSP00000436447.1:n.311-1516T>G
NM_003105.5:c.3581-1516T>G NP_003096.1:n.3581-1516T>G
XM_011542963.1:c.3467-1516T>G XP_011541265.1:n.3467-1516T>G
XM_011542964.1:c.3581-1516T>G XP_011541266.1:n.3581-1516T>G
XM_011542965.1:c.2042-1516T>G XP_011541267.1:n.2042-1516T>G
XM_011542966.1:c.941-1516T>G XP_011541268.1:n.941-1516T>G
XM_011542967.1:c.413-1516T>G XP_011541269.1:n.413-1516T>G
XM_011542963.3:c.3467-1516T>G XP_011541265.1:n.3467-1516T>G
XM_011542965.3:c.2042-1516T>G XP_011541267.1:n.2042-1516T>G
XM_011542967.3:c.413-1516T>G XP_011541269.1:n.413-1516T>G
XM_017018169.2:c.3269-1516T>G XP_016873658.1:n.3269-1516T>G
XM_017018170.2:c.3056-1516T>G XP_016873659.1:n.3056-1516T>G
XM_017018171.1:c.3581-1516T>G XP_016873660.1:n.3581-1516T>G
XM_017018172.2:c.941-1516T>G XP_016873661.1:n.941-1516T>G
NM_003105.6:c.3581-1516T>G MANE Select NP_003096.2:n.3581-1516T>G