Canonical Allele Identifier: CA383033903

Gene: SORL1

Linked Data

• MyVariant Identifiers: chr11:g.121424783T>A (hg19) ; chr11:g.121554074T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.121554074T>A , CM000673.2:g.121554074T>A	GRCh38
NC_000011.9:g.121424783T>A , CM000673.1:g.121424783T>A	GRCh37
NC_000011.8:g.120929993T>A	NCBI36
NG_023313.1:g.106823T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000260197.12:c.2404T>A MANE Select	ENSP00000260197.6:p.Leu802Met
ENST00000260197.11:c.2404T>A	ENSP00000260197.6:p.Leu802Met
NM_003105.5:c.2404T>A	NP_003096.1:p.Leu802Met
XM_011542963.1:c.2404T>A	XP_011541265.1:p.Leu802Met
XM_011542964.1:c.2404T>A	XP_011541266.1:p.Leu802Met
XM_011542965.1:c.865T>A	XP_011541267.1:p.Leu289Met
XM_011542963.3:c.2404T>A	XP_011541265.1:p.Leu802Met
XM_011542965.3:c.865T>A	XP_011541267.1:p.Leu289Met
XM_017018169.2:c.2092T>A	XP_016873658.1:p.Leu698Met
XM_017018170.2:c.1879T>A	XP_016873659.1:p.Leu627Met
XM_017018171.1:c.2404T>A	XP_016873660.1:p.Leu802Met
XM_017018172.2:c.-145T>A	XP_016873661.1:n.-145T>A
NM_003105.6:c.2404T>A MANE Select	NP_003096.2:p.Leu802Met