Canonical Allele Identifier: CA383036104
Gene: SORL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.121558788C>A , CM000673.2:g.121558788C>A GRCh38
NC_000011.9:g.121429497C>A , CM000673.1:g.121429497C>A GRCh37
NC_000011.8:g.120934707C>A NCBI36
NG_023313.1:g.111537C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000260197.12:c.2861C>A MANE Select ENSP00000260197.6:p.Ser954Tyr
ENST00000260197.11:c.2861C>A ENSP00000260197.6:p.Ser954Tyr
ENST00000529445.1:n.567C>A
NM_003105.5:c.2861C>A NP_003096.1:p.Ser954Tyr
XM_011542963.1:c.2861C>A XP_011541265.1:p.Ser954Tyr
XM_011542964.1:c.2861C>A XP_011541266.1:p.Ser954Tyr
XM_011542965.1:c.1322C>A XP_011541267.1:p.Ser441Tyr
XM_011542966.1:c.221C>A XP_011541268.1:p.Ser74Tyr
XM_011542963.3:c.2861C>A XP_011541265.1:p.Ser954Tyr
XM_011542965.3:c.1322C>A XP_011541267.1:p.Ser441Tyr
XM_017018169.2:c.2549C>A XP_016873658.1:p.Ser850Tyr
XM_017018170.2:c.2336C>A XP_016873659.1:p.Ser779Tyr
XM_017018171.1:c.2861C>A XP_016873660.1:p.Ser954Tyr
XM_017018172.2:c.221C>A XP_016873661.1:p.Ser74Tyr
NM_003105.6:c.2861C>A MANE Select NP_003096.2:p.Ser954Tyr