Canonical Allele Identifier: CA383025348

Gene: SORL1

Linked Data

• ClinVar Variation Id: 1409565
• ClinVar RCV Id: RCV001913771
• dbSNP Id: rs2134858782
• MyVariant Identifiers: chr11:g.121393673G>A (hg19) ; chr11:g.121522964G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.121522964G>A , CM000673.2:g.121522964G>A	GRCh38
NC_000011.9:g.121393673G>A , CM000673.1:g.121393673G>A	GRCh37
NC_000011.8:g.120898883G>A	NCBI36
NG_023313.1:g.75713G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260197.12:c.1571G>A MANE Select	ENSP00000260197.6:p.Ser524Asn
ENST00000260197.11:c.1571G>A	ENSP00000260197.6:p.Ser524Asn
ENST00000532451.1:n.1523G>A
NM_003105.5:c.1571G>A	NP_003096.1:p.Ser524Asn
XM_011542963.1:c.1571G>A	XP_011541265.1:p.Ser524Asn
XM_011542964.1:c.1571G>A	XP_011541266.1:p.Ser524Asn
XM_011542965.1:c.-52G>A	XP_011541267.1:n.-52G>A
XM_011542963.3:c.1571G>A	XP_011541265.1:p.Ser524Asn
XM_011542965.3:c.-52G>A	XP_011541267.1:n.-52G>A
XM_017018169.2:c.1259G>A	XP_016873658.1:p.Ser420Asn
XM_017018170.2:c.1046G>A	XP_016873659.1:p.Ser349Asn
XM_017018171.1:c.1571G>A	XP_016873660.1:p.Ser524Asn
NM_003105.6:c.1571G>A MANE Select	NP_003096.2:p.Ser524Asn