Canonical Allele Identifier: CA2616496810

Gene: SORL1

Linked Data

• gnomAD v4: 11-121522777-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.121522777C>A , CM000673.2:g.121522777C>A	GRCh38
NC_000011.9:g.121393486C>A , CM000673.1:g.121393486C>A	GRCh37
NC_000011.8:g.120898696C>A	NCBI36
NG_023313.1:g.75526C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260197.12:c.1522+74C>A MANE Select	ENSP00000260197.6:n.1522+74C>A
ENST00000260197.11:c.1522+74C>A	ENSP00000260197.6:n.1522+74C>A
ENST00000532451.1:n.1474+74C>A
NM_003105.5:c.1522+74C>A	NP_003096.1:n.1522+74C>A
XM_011542963.1:c.1522+74C>A	XP_011541265.1:n.1522+74C>A
XM_011542964.1:c.1522+74C>A	XP_011541266.1:n.1522+74C>A
XM_011542965.1:c.-101+74C>A	XP_011541267.1:n.-101+74C>A
XM_011542963.3:c.1522+74C>A	XP_011541265.1:n.1522+74C>A
XM_011542965.3:c.-101+74C>A	XP_011541267.1:n.-101+74C>A
XM_017018169.2:c.1210+74C>A	XP_016873658.1:n.1210+74C>A
XM_017018170.2:c.997+74C>A	XP_016873659.1:n.997+74C>A
XM_017018171.1:c.1522+74C>A	XP_016873660.1:n.1522+74C>A
NM_003105.6:c.1522+74C>A MANE Select	NP_003096.2:n.1522+74C>A