Canonical Allele Identifier: CA383024502

Gene: SORL1

Linked Data

• MyVariant Identifiers: chr11:g.121393323C>A (hg19) ; chr11:g.121522614C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.121522614C>A , CM000673.2:g.121522614C>A	GRCh38
NC_000011.9:g.121393323C>A , CM000673.1:g.121393323C>A	GRCh37
NC_000011.8:g.120898533C>A	NCBI36
NG_023313.1:g.75363C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260197.12:c.1433C>A MANE Select	ENSP00000260197.6:p.Ala478Asp
ENST00000260197.11:c.1433C>A	ENSP00000260197.6:p.Ala478Asp
ENST00000532451.1:n.1385C>A
NM_003105.5:c.1433C>A	NP_003096.1:p.Ala478Asp
XM_011542963.1:c.1433C>A	XP_011541265.1:p.Ala478Asp
XM_011542964.1:c.1433C>A	XP_011541266.1:p.Ala478Asp
XM_011542965.1:c.-190C>A	XP_011541267.1:n.-190C>A
XM_011542963.3:c.1433C>A	XP_011541265.1:p.Ala478Asp
XM_011542965.3:c.-190C>A	XP_011541267.1:n.-190C>A
XM_017018169.2:c.1121C>A	XP_016873658.1:p.Ala374Asp
XM_017018170.2:c.908C>A	XP_016873659.1:p.Ala303Asp
XM_017018171.1:c.1433C>A	XP_016873660.1:p.Ala478Asp
NM_003105.6:c.1433C>A MANE Select	NP_003096.2:p.Ala478Asp