Canonical Allele Identifier: CA477218103
Gene: SORL1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.121393378C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.121522669C>G , CM000673.2:g.121522669C>G GRCh38
NC_000011.9:g.121393378C>G , CM000673.1:g.121393378C>G GRCh37
NC_000011.8:g.120898588C>G NCBI36
NG_023313.1:g.75418C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000260197.12:c.1488C>G MANE Select ENSP00000260197.6:p.Ser496=
ENST00000260197.11:c.1488C>G ENSP00000260197.6:p.Ser496=
ENST00000532451.1:n.1440C>G
NM_003105.5:c.1488C>G NP_003096.1:p.Ser496=
XM_011542963.1:c.1488C>G XP_011541265.1:p.Ser496=
XM_011542964.1:c.1488C>G XP_011541266.1:p.Ser496=
XM_011542965.1:c.-135C>G XP_011541267.1:n.-135C>G
XM_011542963.3:c.1488C>G XP_011541265.1:p.Ser496=
XM_011542965.3:c.-135C>G XP_011541267.1:n.-135C>G
XM_017018169.2:c.1176C>G XP_016873658.1:p.Ser392=
XM_017018170.2:c.963C>G XP_016873659.1:p.Ser321=
XM_017018171.1:c.1488C>G XP_016873660.1:p.Ser496=
NM_003105.6:c.1488C>G MANE Select NP_003096.2:p.Ser496=