Canonical Allele Identifier: CA2616500863

Gene: SORL1

Linked Data

• gnomAD v4: 11-121586170-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.121586170G>A , CM000673.2:g.121586170G>A	GRCh38
NC_000011.9:g.121456879G>A , CM000673.1:g.121456879G>A	GRCh37
NC_000011.8:g.120962089G>A	NCBI36
NG_023313.1:g.138919G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000260197.12:c.3707-52G>A MANE Select	ENSP00000260197.6:n.3707-52G>A
ENST00000260197.11:c.3707-52G>A	ENSP00000260197.6:n.3707-52G>A
ENST00000525532.5:c.539-52G>A	ENSP00000434634.1:n.539-52G>A
ENST00000532694.5:c.245-52G>A	ENSP00000432131.1:n.245-52G>A
ENST00000534286.5:c.437-52G>A	ENSP00000436447.1:n.437-52G>A
NM_003105.5:c.3707-52G>A	NP_003096.1:n.3707-52G>A
XM_011542963.1:c.3593-52G>A	XP_011541265.1:n.3593-52G>A
XM_011542964.1:c.3707-52G>A	XP_011541266.1:n.3707-52G>A
XM_011542965.1:c.2168-52G>A	XP_011541267.1:n.2168-52G>A
XM_011542966.1:c.1067-52G>A	XP_011541268.1:n.1067-52G>A
XM_011542967.1:c.539-52G>A	XP_011541269.1:n.539-52G>A
XM_011542963.3:c.3593-52G>A	XP_011541265.1:n.3593-52G>A
XM_011542965.3:c.2168-52G>A	XP_011541267.1:n.2168-52G>A
XM_011542967.3:c.539-52G>A	XP_011541269.1:n.539-52G>A
XM_017018169.2:c.3395-52G>A	XP_016873658.1:n.3395-52G>A
XM_017018170.2:c.3182-52G>A	XP_016873659.1:n.3182-52G>A
XM_017018171.1:c.3707-52G>A	XP_016873660.1:n.3707-52G>A
XM_017018172.2:c.1067-52G>A	XP_016873661.1:n.1067-52G>A
NM_003105.6:c.3707-52G>A MANE Select	NP_003096.2:n.3707-52G>A