Canonical Allele Identifier: CA383036061
Gene: SORL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.121558770T>C , CM000673.2:g.121558770T>C GRCh38
NC_000011.9:g.121429479T>C , CM000673.1:g.121429479T>C GRCh37
NC_000011.8:g.120934689T>C NCBI36
NG_023313.1:g.111519T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000260197.12:c.2843T>C MANE Select ENSP00000260197.6:p.Phe948Ser
ENST00000260197.11:c.2843T>C ENSP00000260197.6:p.Phe948Ser
ENST00000524873.1:n.571T>C
ENST00000529445.1:n.549T>C
NM_003105.5:c.2843T>C NP_003096.1:p.Phe948Ser
XM_011542963.1:c.2843T>C XP_011541265.1:p.Phe948Ser
XM_011542964.1:c.2843T>C XP_011541266.1:p.Phe948Ser
XM_011542965.1:c.1304T>C XP_011541267.1:p.Phe435Ser
XM_011542966.1:c.203T>C XP_011541268.1:p.Phe68Ser
XM_011542963.3:c.2843T>C XP_011541265.1:p.Phe948Ser
XM_011542965.3:c.1304T>C XP_011541267.1:p.Phe435Ser
XM_017018169.2:c.2531T>C XP_016873658.1:p.Phe844Ser
XM_017018170.2:c.2318T>C XP_016873659.1:p.Phe773Ser
XM_017018171.1:c.2843T>C XP_016873660.1:p.Phe948Ser
XM_017018172.2:c.203T>C XP_016873661.1:p.Phe68Ser
NM_003105.6:c.2843T>C MANE Select NP_003096.2:p.Phe948Ser