Canonical Allele Identifier: CA383033736

Gene: SORL1

Linked Data

• MyVariant Identifiers: chr11:g.121424702G>A (hg19) ; chr11:g.121553993G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.121553993G>A , CM000673.2:g.121553993G>A	GRCh38
NC_000011.9:g.121424702G>A , CM000673.1:g.121424702G>A	GRCh37
NC_000011.8:g.120929912G>A	NCBI36
NG_023313.1:g.106742G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260197.12:c.2323G>A MANE Select	ENSP00000260197.6:p.Ala775Thr
ENST00000260197.11:c.2323G>A	ENSP00000260197.6:p.Ala775Thr
NM_003105.5:c.2323G>A	NP_003096.1:p.Ala775Thr
XM_011542963.1:c.2323G>A	XP_011541265.1:p.Ala775Thr
XM_011542964.1:c.2323G>A	XP_011541266.1:p.Ala775Thr
XM_011542965.1:c.784G>A	XP_011541267.1:p.Ala262Thr
XM_011542963.3:c.2323G>A	XP_011541265.1:p.Ala775Thr
XM_011542965.3:c.784G>A	XP_011541267.1:p.Ala262Thr
XM_017018169.2:c.2011G>A	XP_016873658.1:p.Ala671Thr
XM_017018170.2:c.1798G>A	XP_016873659.1:p.Ala600Thr
XM_017018171.1:c.2323G>A	XP_016873660.1:p.Ala775Thr
XM_017018172.2:c.-226G>A	XP_016873661.1:n.-226G>A
NM_003105.6:c.2323G>A MANE Select	NP_003096.2:p.Ala775Thr