Canonical Allele Identifier: CA2004951349
Gene: SORL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.121586172C= , CM000673.2:g.121586172C= GRCh38
NC_000011.9:g.121456881C= , CM000673.1:g.121456881C= GRCh37
NC_000011.8:g.120962091C= NCBI36
NG_023313.1:g.138921C=

Transcript Alleles

HGVS Amino-acid change
ENST00000260197.12:c.3707-50C= MANE Select ENSP00000260197.6:n.3707-50C=
ENST00000260197.11:c.3707-50C= ENSP00000260197.6:n.3707-50C=
ENST00000525532.5:c.539-50C= ENSP00000434634.1:n.539-50C=
ENST00000532694.5:c.245-50C= ENSP00000432131.1:n.245-50C=
ENST00000534286.5:c.437-50C= ENSP00000436447.1:n.437-50C=
NM_003105.5:c.3707-50C= NP_003096.1:n.3707-50C=
XM_011542963.1:c.3593-50C= XP_011541265.1:n.3593-50C=
XM_011542964.1:c.3707-50C= XP_011541266.1:n.3707-50C=
XM_011542965.1:c.2168-50C= XP_011541267.1:n.2168-50C=
XM_011542966.1:c.1067-50C= XP_011541268.1:n.1067-50C=
XM_011542967.1:c.539-50C= XP_011541269.1:n.539-50C=
XM_011542963.3:c.3593-50C= XP_011541265.1:n.3593-50C=
XM_011542965.3:c.2168-50C= XP_011541267.1:n.2168-50C=
XM_011542967.3:c.539-50C= XP_011541269.1:n.539-50C=
XM_017018169.2:c.3395-50C= XP_016873658.1:n.3395-50C=
XM_017018170.2:c.3182-50C= XP_016873659.1:n.3182-50C=
XM_017018171.1:c.3707-50C= XP_016873660.1:n.3707-50C=
XM_017018172.2:c.1067-50C= XP_016873661.1:n.1067-50C=
NM_003105.6:c.3707-50C= MANE Select NP_003096.2:n.3707-50C=