Canonical Allele Identifier: CA2725072846
Gene: SORL1 HGNC NCBI

Linked Data

dbSNP Id: rs2134827746

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.121500374T>C , CM000673.2:g.121500374T>C GRCh38
NC_000011.9:g.121371083T>C , CM000673.1:g.121371083T>C GRCh37
NC_000011.8:g.120876293T>C NCBI36
NG_023313.1:g.53123T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000260197.12:c.939+3325T>C MANE Select ENSP00000260197.6:n.939+3325T>C
ENST00000260197.11:c.939+3325T>C ENSP00000260197.6:n.939+3325T>C
ENST00000532451.1:n.891+3325T>C
NM_003105.5:c.939+3325T>C NP_003096.1:n.939+3325T>C
XM_011542963.1:c.939+3325T>C XP_011541265.1:n.939+3325T>C
XM_011542964.1:c.939+3325T>C XP_011541266.1:n.939+3325T>C
XM_011542963.3:c.939+3325T>C XP_011541265.1:n.939+3325T>C
XM_011542965.3:c.-684+3325T>C XP_011541267.1:n.-684+3325T>C
XM_017018169.2:c.627+3325T>C XP_016873658.1:n.627+3325T>C
XM_017018170.2:c.414+3325T>C XP_016873659.1:n.414+3325T>C
XM_017018171.1:c.939+3325T>C XP_016873660.1:n.939+3325T>C
NM_003105.6:c.939+3325T>C MANE Select NP_003096.2:n.939+3325T>C