Canonical Allele Identifier: CA383035650

Gene: SORL1

Linked Data

• MyVariant Identifiers: chr11:g.121429323G>A (hg19) ; chr11:g.121558614G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.121558614G>A , CM000673.2:g.121558614G>A	GRCh38
NC_000011.9:g.121429323G>A , CM000673.1:g.121429323G>A	GRCh37
NC_000011.8:g.120934533G>A	NCBI36
NG_023313.1:g.111363G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260197.12:c.2687G>A MANE Select	ENSP00000260197.6:p.Gly896Glu
ENST00000260197.11:c.2687G>A	ENSP00000260197.6:p.Gly896Glu
ENST00000524873.1:n.415G>A
ENST00000529445.1:n.393G>A
NM_003105.5:c.2687G>A	NP_003096.1:p.Gly896Glu
XM_011542963.1:c.2687G>A	XP_011541265.1:p.Gly896Glu
XM_011542964.1:c.2687G>A	XP_011541266.1:p.Gly896Glu
XM_011542965.1:c.1148G>A	XP_011541267.1:p.Gly383Glu
XM_011542966.1:c.47G>A	XP_011541268.1:p.Gly16Glu
XM_011542963.3:c.2687G>A	XP_011541265.1:p.Gly896Glu
XM_011542965.3:c.1148G>A	XP_011541267.1:p.Gly383Glu
XM_017018169.2:c.2375G>A	XP_016873658.1:p.Gly792Glu
XM_017018170.2:c.2162G>A	XP_016873659.1:p.Gly721Glu
XM_017018171.1:c.2687G>A	XP_016873660.1:p.Gly896Glu
XM_017018172.2:c.47G>A	XP_016873661.1:p.Gly16Glu
NM_003105.6:c.2687G>A MANE Select	NP_003096.2:p.Gly896Glu