Canonical Allele Identifier: CA6328623

Gene: SORL1

Linked Data

• dbSNP Id: rs778558596
• ExAC: 11:121393302 A / G
• gnomAD v2: 11-121393302-A-G
• gnomAD v4: 11-121522593-A-G
• MyVariant Identifiers: chr11:g.121393302A>G (hg19) ; chr11:g.121522593A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.121522593A>G , CM000673.2:g.121522593A>G	GRCh38
NC_000011.9:g.121393302A>G , CM000673.1:g.121393302A>G	GRCh37
NC_000011.8:g.120898512A>G	NCBI36
NG_023313.1:g.75342A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260197.12:c.1412A>G MANE Select	ENSP00000260197.6:p.Gln471Arg
ENST00000260197.11:c.1412A>G	ENSP00000260197.6:p.Gln471Arg
ENST00000532451.1:n.1364A>G
NM_003105.5:c.1412A>G	NP_003096.1:p.Gln471Arg
XM_011542963.1:c.1412A>G	XP_011541265.1:p.Gln471Arg
XM_011542964.1:c.1412A>G	XP_011541266.1:p.Gln471Arg
XM_011542965.1:c.-211A>G	XP_011541267.1:n.-211A>G
XM_011542963.3:c.1412A>G	XP_011541265.1:p.Gln471Arg
XM_011542965.3:c.-211A>G	XP_011541267.1:n.-211A>G
XM_017018169.2:c.1100A>G	XP_016873658.1:p.Gln367Arg
XM_017018170.2:c.887A>G	XP_016873659.1:p.Gln296Arg
XM_017018171.1:c.1412A>G	XP_016873660.1:p.Gln471Arg
NM_003105.6:c.1412A>G MANE Select	NP_003096.2:p.Gln471Arg