Canonical Allele Identifier: CA2004922204
Gene: SORL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.121605218G= , CM000673.2:g.121605218G= GRCh38
NC_000011.9:g.121475927G= , CM000673.1:g.121475927G= GRCh37
NC_000011.8:g.120981137G= NCBI36
NG_023313.1:g.157967G=

Transcript Alleles

HGVS Amino-acid change
ENST00000260197.12:c.4757G= MANE Select ENSP00000260197.6:p.Cys1586=
ENST00000260197.11:c.4757G= ENSP00000260197.6:p.Cys1586=
ENST00000525532.5:c.1589G= ENSP00000434634.1:p.Cys530=
ENST00000527934.1:c.602G= ENSP00000435405.1:p.Cys201=
ENST00000532694.5:c.1295G= ENSP00000432131.1:p.Cys432=
ENST00000534286.5:c.1487G= ENSP00000436447.1:p.Cys496=
NM_003105.5:c.4757G= NP_003096.1:p.Cys1586=
XM_011542963.1:c.4643G= XP_011541265.1:p.Cys1548=
XM_011542964.1:c.4757G= XP_011541266.1:p.Cys1586=
XM_011542965.1:c.3218G= XP_011541267.1:p.Cys1073=
XM_011542966.1:c.2117G= XP_011541268.1:p.Cys706=
XM_011542967.1:c.1589G= XP_011541269.1:p.Cys530=
XM_011542963.3:c.4643G= XP_011541265.1:p.Cys1548=
XM_011542965.3:c.3218G= XP_011541267.1:p.Cys1073=
XM_011542967.3:c.1589G= XP_011541269.1:p.Cys530=
XM_017018169.2:c.4445G= XP_016873658.1:p.Cys1482=
XM_017018170.2:c.4232G= XP_016873659.1:p.Cys1411=
XM_017018171.1:c.4757G= XP_016873660.1:p.Cys1586=
XM_017018172.2:c.2117G= XP_016873661.1:p.Cys706=
NM_003105.6:c.4757G= MANE Select NP_003096.2:p.Cys1586=