Canonical Allele Identifier: CA2004910543
Gene: SORL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.121522738G= , CM000673.2:g.121522738G= GRCh38
NC_000011.9:g.121393447G= , CM000673.1:g.121393447G= GRCh37
NC_000011.8:g.120898657G= NCBI36
NG_023313.1:g.75487G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260197.12:c.1522+35G= MANE Select ENSP00000260197.6:n.1522+35G=
ENST00000260197.11:c.1522+35G= ENSP00000260197.6:n.1522+35G=
ENST00000532451.1:n.1474+35G=
NM_003105.5:c.1522+35G= NP_003096.1:n.1522+35G=
XM_011542963.1:c.1522+35G= XP_011541265.1:n.1522+35G=
XM_011542964.1:c.1522+35G= XP_011541266.1:n.1522+35G=
XM_011542965.1:c.-101+35G= XP_011541267.1:n.-101+35G=
XM_011542963.3:c.1522+35G= XP_011541265.1:n.1522+35G=
XM_011542965.3:c.-101+35G= XP_011541267.1:n.-101+35G=
XM_017018169.2:c.1210+35G= XP_016873658.1:n.1210+35G=
XM_017018170.2:c.997+35G= XP_016873659.1:n.997+35G=
XM_017018171.1:c.1522+35G= XP_016873660.1:n.1522+35G=
NM_003105.6:c.1522+35G= MANE Select NP_003096.2:n.1522+35G=