Canonical Allele Identifier: CA383038422

Gene: SORL1

Linked Data

• MyVariant Identifiers: chr11:g.121475845C>G (hg19) ; chr11:g.121605136C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.121605136C>G , CM000673.2:g.121605136C>G	GRCh38
NC_000011.9:g.121475845C>G , CM000673.1:g.121475845C>G	GRCh37
NC_000011.8:g.120981055C>G	NCBI36
NG_023313.1:g.157885C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000260197.12:c.4675C>G MANE Select	ENSP00000260197.6:p.Gln1559Glu
ENST00000260197.11:c.4675C>G	ENSP00000260197.6:p.Gln1559Glu
ENST00000525532.5:c.1507C>G	ENSP00000434634.1:p.Gln503Glu
ENST00000527934.1:c.520C>G	ENSP00000435405.1:p.Gln174Glu
ENST00000532694.5:c.1213C>G	ENSP00000432131.1:p.Gln405Glu
ENST00000534286.5:c.1405C>G	ENSP00000436447.1:p.Gln469Glu
NM_003105.5:c.4675C>G	NP_003096.1:p.Gln1559Glu
XM_011542963.1:c.4561C>G	XP_011541265.1:p.Gln1521Glu
XM_011542964.1:c.4675C>G	XP_011541266.1:p.Gln1559Glu
XM_011542965.1:c.3136C>G	XP_011541267.1:p.Gln1046Glu
XM_011542966.1:c.2035C>G	XP_011541268.1:p.Gln679Glu
XM_011542967.1:c.1507C>G	XP_011541269.1:p.Gln503Glu
XM_011542963.3:c.4561C>G	XP_011541265.1:p.Gln1521Glu
XM_011542965.3:c.3136C>G	XP_011541267.1:p.Gln1046Glu
XM_011542967.3:c.1507C>G	XP_011541269.1:p.Gln503Glu
XM_017018169.2:c.4363C>G	XP_016873658.1:p.Gln1455Glu
XM_017018170.2:c.4150C>G	XP_016873659.1:p.Gln1384Glu
XM_017018171.1:c.4675C>G	XP_016873660.1:p.Gln1559Glu
XM_017018172.2:c.2035C>G	XP_016873661.1:p.Gln679Glu
NM_003105.6:c.4675C>G MANE Select	NP_003096.2:p.Gln1559Glu