Canonical Allele Identifier: CA2616496832

Gene: SORL1

Linked Data

• gnomAD v4: 11-121522835-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.121522835C>G , CM000673.2:g.121522835C>G	GRCh38
NC_000011.9:g.121393544C>G , CM000673.1:g.121393544C>G	GRCh37
NC_000011.8:g.120898754C>G	NCBI36
NG_023313.1:g.75584C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260197.12:c.1523-81C>G MANE Select	ENSP00000260197.6:n.1523-81C>G
ENST00000260197.11:c.1523-81C>G	ENSP00000260197.6:n.1523-81C>G
ENST00000532451.1:n.1475-81C>G
NM_003105.5:c.1523-81C>G	NP_003096.1:n.1523-81C>G
XM_011542963.1:c.1523-81C>G	XP_011541265.1:n.1523-81C>G
XM_011542964.1:c.1523-81C>G	XP_011541266.1:n.1523-81C>G
XM_011542965.1:c.-100-81C>G	XP_011541267.1:n.-100-81C>G
XM_011542963.3:c.1523-81C>G	XP_011541265.1:n.1523-81C>G
XM_011542965.3:c.-100-81C>G	XP_011541267.1:n.-100-81C>G
XM_017018169.2:c.1211-81C>G	XP_016873658.1:n.1211-81C>G
XM_017018170.2:c.998-81C>G	XP_016873659.1:n.998-81C>G
XM_017018171.1:c.1523-81C>G	XP_016873660.1:n.1523-81C>G
NM_003105.6:c.1523-81C>G MANE Select	NP_003096.2:n.1523-81C>G