Canonical Allele Identifier: CA6329723
Gene: SORL1 HGNC NCBI

Linked Data

dbSNP Id: rs373079871

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.121605113A>G , CM000673.2:g.121605113A>G GRCh38
NC_000011.9:g.121475822A>G , CM000673.1:g.121475822A>G GRCh37
NC_000011.8:g.120981032A>G NCBI36
NG_023313.1:g.157862A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000260197.12:c.4652A>G MANE Select ENSP00000260197.6:p.Asp1551Gly
ENST00000260197.11:c.4652A>G ENSP00000260197.6:p.Asp1551Gly
ENST00000525532.5:c.1484A>G ENSP00000434634.1:p.Asp495Gly
ENST00000527934.1:c.497A>G ENSP00000435405.1:p.Asp166Gly
ENST00000532694.5:c.1190A>G ENSP00000432131.1:p.Asp397Gly
ENST00000534286.5:c.1382A>G ENSP00000436447.1:p.Asp461Gly
NM_003105.5:c.4652A>G NP_003096.1:p.Asp1551Gly
XM_011542963.1:c.4538A>G XP_011541265.1:p.Asp1513Gly
XM_011542964.1:c.4652A>G XP_011541266.1:p.Asp1551Gly
XM_011542965.1:c.3113A>G XP_011541267.1:p.Asp1038Gly
XM_011542966.1:c.2012A>G XP_011541268.1:p.Asp671Gly
XM_011542967.1:c.1484A>G XP_011541269.1:p.Asp495Gly
XM_011542963.3:c.4538A>G XP_011541265.1:p.Asp1513Gly
XM_011542965.3:c.3113A>G XP_011541267.1:p.Asp1038Gly
XM_011542967.3:c.1484A>G XP_011541269.1:p.Asp495Gly
XM_017018169.2:c.4340A>G XP_016873658.1:p.Asp1447Gly
XM_017018170.2:c.4127A>G XP_016873659.1:p.Asp1376Gly
XM_017018171.1:c.4652A>G XP_016873660.1:p.Asp1551Gly
XM_017018172.2:c.2012A>G XP_016873661.1:p.Asp671Gly
NM_003105.6:c.4652A>G MANE Select NP_003096.2:p.Asp1551Gly