Canonical Allele Identifier: CA383024763

Gene: SORL1

Linked Data

• gnomAD v4: 11-121522698-C-T
• MyVariant Identifiers: chr11:g.121393407C>T (hg19) ; chr11:g.121522698C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.121522698C>T , CM000673.2:g.121522698C>T	GRCh38
NC_000011.9:g.121393407C>T , CM000673.1:g.121393407C>T	GRCh37
NC_000011.8:g.120898617C>T	NCBI36
NG_023313.1:g.75447C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260197.12:c.1517C>T MANE Select	ENSP00000260197.6:p.Ala506Val
ENST00000260197.11:c.1517C>T	ENSP00000260197.6:p.Ala506Val
ENST00000532451.1:n.1469C>T
NM_003105.5:c.1517C>T	NP_003096.1:p.Ala506Val
XM_011542963.1:c.1517C>T	XP_011541265.1:p.Ala506Val
XM_011542964.1:c.1517C>T	XP_011541266.1:p.Ala506Val
XM_011542965.1:c.-106C>T	XP_011541267.1:n.-106C>T
XM_011542963.3:c.1517C>T	XP_011541265.1:p.Ala506Val
XM_011542965.3:c.-106C>T	XP_011541267.1:n.-106C>T
XM_017018169.2:c.1205C>T	XP_016873658.1:p.Ala402Val
XM_017018170.2:c.992C>T	XP_016873659.1:p.Ala331Val
XM_017018171.1:c.1517C>T	XP_016873660.1:p.Ala506Val
NM_003105.6:c.1517C>T MANE Select	NP_003096.2:p.Ala506Val