Canonical Allele Identifier: CA2793900948
Gene: SORL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.121505113G>A , CM000673.2:g.121505113G>A GRCh38
NC_000011.9:g.121375822G>A , CM000673.1:g.121375822G>A GRCh37
NC_000011.8:g.120881032G>A NCBI36
NG_023313.1:g.57862G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000260197.12:c.940-7890G>A MANE Select ENSP00000260197.6:n.940-7890G>A
ENST00000260197.11:c.940-7890G>A ENSP00000260197.6:n.940-7890G>A
ENST00000532451.1:n.892-7890G>A
NM_003105.5:c.940-7890G>A NP_003096.1:n.940-7890G>A
XM_011542963.1:c.940-7890G>A XP_011541265.1:n.940-7890G>A
XM_011542964.1:c.940-7890G>A XP_011541266.1:n.940-7890G>A
XM_011542963.3:c.940-7890G>A XP_011541265.1:n.940-7890G>A
XM_011542965.3:c.-683-7890G>A XP_011541267.1:n.-683-7890G>A
XM_017018169.2:c.628-7890G>A XP_016873658.1:n.628-7890G>A
XM_017018170.2:c.415-7890G>A XP_016873659.1:n.415-7890G>A
XM_017018171.1:c.940-7890G>A XP_016873660.1:n.940-7890G>A
NM_003105.6:c.940-7890G>A MANE Select NP_003096.2:n.940-7890G>A