Canonical Allele Identifier: CA2004951388
Gene: SORL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.121586266C= , CM000673.2:g.121586266C= GRCh38
NC_000011.9:g.121456975C= , CM000673.1:g.121456975C= GRCh37
NC_000011.8:g.120962185C= NCBI36
NG_023313.1:g.139015C=

Transcript Alleles

HGVS Amino-acid change
ENST00000260197.12:c.3751C= MANE Select ENSP00000260197.6:p.Pro1251=
ENST00000260197.11:c.3751C= ENSP00000260197.6:p.Pro1251=
ENST00000525532.5:c.583C= ENSP00000434634.1:p.Pro195=
ENST00000532694.5:c.289C= ENSP00000432131.1:p.Pro97=
ENST00000534286.5:c.481C= ENSP00000436447.1:p.Pro161=
NM_003105.5:c.3751C= NP_003096.1:p.Pro1251=
XM_011542963.1:c.3637C= XP_011541265.1:p.Pro1213=
XM_011542964.1:c.3751C= XP_011541266.1:p.Pro1251=
XM_011542965.1:c.2212C= XP_011541267.1:p.Pro738=
XM_011542966.1:c.1111C= XP_011541268.1:p.Pro371=
XM_011542967.1:c.583C= XP_011541269.1:p.Pro195=
XM_011542963.3:c.3637C= XP_011541265.1:p.Pro1213=
XM_011542965.3:c.2212C= XP_011541267.1:p.Pro738=
XM_011542967.3:c.583C= XP_011541269.1:p.Pro195=
XM_017018169.2:c.3439C= XP_016873658.1:p.Pro1147=
XM_017018170.2:c.3226C= XP_016873659.1:p.Pro1076=
XM_017018171.1:c.3751C= XP_016873660.1:p.Pro1251=
XM_017018172.2:c.1111C= XP_016873661.1:p.Pro371=
NM_003105.6:c.3751C= MANE Select NP_003096.2:p.Pro1251=