Canonical Allele Identifier: CA477218043
Gene: SORL1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.121393297T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.121522588T>C , CM000673.2:g.121522588T>C GRCh38
NC_000011.9:g.121393297T>C , CM000673.1:g.121393297T>C GRCh37
NC_000011.8:g.120898507T>C NCBI36
NG_023313.1:g.75337T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000260197.12:c.1407T>C MANE Select ENSP00000260197.6:p.Leu469=
ENST00000260197.11:c.1407T>C ENSP00000260197.6:p.Leu469=
ENST00000532451.1:n.1359T>C
NM_003105.5:c.1407T>C NP_003096.1:p.Leu469=
XM_011542963.1:c.1407T>C XP_011541265.1:p.Leu469=
XM_011542964.1:c.1407T>C XP_011541266.1:p.Leu469=
XM_011542965.1:c.-216T>C XP_011541267.1:n.-216T>C
XM_011542963.3:c.1407T>C XP_011541265.1:p.Leu469=
XM_011542965.3:c.-216T>C XP_011541267.1:n.-216T>C
XM_017018169.2:c.1095T>C XP_016873658.1:p.Leu365=
XM_017018170.2:c.882T>C XP_016873659.1:p.Leu294=
XM_017018171.1:c.1407T>C XP_016873660.1:p.Leu469=
NM_003105.6:c.1407T>C MANE Select NP_003096.2:p.Leu469=