Canonical Allele Identifier: CA383036135

Gene: SORL1

Linked Data

• gnomAD v4: 11-121558804-C-A
• MyVariant Identifiers: chr11:g.121429513C>A (hg19) ; chr11:g.121558804C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.121558804C>A , CM000673.2:g.121558804C>A	GRCh38
NC_000011.9:g.121429513C>A , CM000673.1:g.121429513C>A	GRCh37
NC_000011.8:g.120934723C>A	NCBI36
NG_023313.1:g.111553C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260197.12:c.2877C>A MANE Select	ENSP00000260197.6:p.Asn959Lys
ENST00000260197.11:c.2877C>A	ENSP00000260197.6:p.Asn959Lys
ENST00000529445.1:n.583C>A
NM_003105.5:c.2877C>A	NP_003096.1:p.Asn959Lys
XM_011542963.1:c.2877C>A	XP_011541265.1:p.Asn959Lys
XM_011542964.1:c.2877C>A	XP_011541266.1:p.Asn959Lys
XM_011542965.1:c.1338C>A	XP_011541267.1:p.Asn446Lys
XM_011542966.1:c.237C>A	XP_011541268.1:p.Asn79Lys
XM_011542963.3:c.2877C>A	XP_011541265.1:p.Asn959Lys
XM_011542965.3:c.1338C>A	XP_011541267.1:p.Asn446Lys
XM_017018169.2:c.2565C>A	XP_016873658.1:p.Asn855Lys
XM_017018170.2:c.2352C>A	XP_016873659.1:p.Asn784Lys
XM_017018171.1:c.2877C>A	XP_016873660.1:p.Asn959Lys
XM_017018172.2:c.237C>A	XP_016873661.1:p.Asn79Lys
NM_003105.6:c.2877C>A MANE Select	NP_003096.2:p.Asn959Lys