Canonical Allele Identifier: CA477219353

Gene: SORL1

Linked Data

• gnomAD v4: 11-121577381-T-A
• MyVariant Identifiers: chr11:g.121448090T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.121577381T>A , CM000673.2:g.121577381T>A	GRCh38
NC_000011.9:g.121448090T>A , CM000673.1:g.121448090T>A	GRCh37
NC_000011.8:g.120953300T>A	NCBI36
NG_023313.1:g.130130T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260197.12:c.3561T>A MANE Select	ENSP00000260197.6:p.Ser1187=
ENST00000260197.11:c.3561T>A	ENSP00000260197.6:p.Ser1187=
ENST00000525532.5:c.393T>A	ENSP00000434634.1:p.Ser131=
ENST00000532694.5:c.99T>A	ENSP00000432131.1:p.Ser33=
ENST00000534286.5:c.291T>A	ENSP00000436447.1:p.Ser97=
NM_003105.5:c.3561T>A	NP_003096.1:p.Ser1187=
XM_011542963.1:c.3447T>A	XP_011541265.1:p.Ser1149=
XM_011542964.1:c.3561T>A	XP_011541266.1:p.Ser1187=
XM_011542965.1:c.2022T>A	XP_011541267.1:p.Ser674=
XM_011542966.1:c.921T>A	XP_011541268.1:p.Ser307=
XM_011542967.1:c.393T>A	XP_011541269.1:p.Ser131=
XM_011542963.3:c.3447T>A	XP_011541265.1:p.Ser1149=
XM_011542965.3:c.2022T>A	XP_011541267.1:p.Ser674=
XM_011542967.3:c.393T>A	XP_011541269.1:p.Ser131=
XM_017018169.2:c.3249T>A	XP_016873658.1:p.Ser1083=
XM_017018170.2:c.3036T>A	XP_016873659.1:p.Ser1012=
XM_017018171.1:c.3561T>A	XP_016873660.1:p.Ser1187=
XM_017018172.2:c.921T>A	XP_016873661.1:p.Ser307=
NM_003105.6:c.3561T>A MANE Select	NP_003096.2:p.Ser1187=