Canonical Allele Identifier: CA2004951383
Gene: SORL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.121586253C= , CM000673.2:g.121586253C= GRCh38
NC_000011.9:g.121456962C= , CM000673.1:g.121456962C= GRCh37
NC_000011.8:g.120962172C= NCBI36
NG_023313.1:g.139002C=

Transcript Alleles

HGVS Amino-acid change
ENST00000260197.12:c.3738C= MANE Select ENSP00000260197.6:p.Asn1246=
ENST00000260197.11:c.3738C= ENSP00000260197.6:p.Asn1246=
ENST00000525532.5:c.570C= ENSP00000434634.1:p.Asn190=
ENST00000532694.5:c.276C= ENSP00000432131.1:p.Asn92=
ENST00000534286.5:c.468C= ENSP00000436447.1:p.Asn156=
NM_003105.5:c.3738C= NP_003096.1:p.Asn1246=
XM_011542963.1:c.3624C= XP_011541265.1:p.Asn1208=
XM_011542964.1:c.3738C= XP_011541266.1:p.Asn1246=
XM_011542965.1:c.2199C= XP_011541267.1:p.Asn733=
XM_011542966.1:c.1098C= XP_011541268.1:p.Asn366=
XM_011542967.1:c.570C= XP_011541269.1:p.Asn190=
XM_011542963.3:c.3624C= XP_011541265.1:p.Asn1208=
XM_011542965.3:c.2199C= XP_011541267.1:p.Asn733=
XM_011542967.3:c.570C= XP_011541269.1:p.Asn190=
XM_017018169.2:c.3426C= XP_016873658.1:p.Asn1142=
XM_017018170.2:c.3213C= XP_016873659.1:p.Asn1071=
XM_017018171.1:c.3738C= XP_016873660.1:p.Asn1246=
XM_017018172.2:c.1098C= XP_016873661.1:p.Asn366=
NM_003105.6:c.3738C= MANE Select NP_003096.2:p.Asn1246=