Canonical Allele Identifier: CA672604566

Gene: SORL1

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.121594237A>T , CM000673.2:g.121594237A>T	GRCh38
NC_000011.9:g.121464946A>T , CM000673.1:g.121464946A>T	GRCh37
NC_000011.8:g.120970156A>T	NCBI36
NG_023313.1:g.146986A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260197.12:c.4370-1386A>T MANE Select	ENSP00000260197.6:n.4370-1386A>T
ENST00000260197.11:c.4370-1386A>T	ENSP00000260197.6:n.4370-1386A>T
ENST00000525532.5:c.1202-1386A>T	ENSP00000434634.1:n.1202-1386A>T
ENST00000527934.1:c.215-1386A>T	ENSP00000435405.1:n.215-1386A>T
ENST00000532694.5:c.908-1386A>T	ENSP00000432131.1:n.908-1386A>T
ENST00000534286.5:c.1100-1386A>T	ENSP00000436447.1:n.1100-1386A>T
NM_003105.5:c.4370-1386A>T	NP_003096.1:n.4370-1386A>T
XM_011542963.1:c.4256-1386A>T	XP_011541265.1:n.4256-1386A>T
XM_011542964.1:c.4370-1386A>T	XP_011541266.1:n.4370-1386A>T
XM_011542965.1:c.2831-1386A>T	XP_011541267.1:n.2831-1386A>T
XM_011542966.1:c.1730-1386A>T	XP_011541268.1:n.1730-1386A>T
XM_011542967.1:c.1202-1386A>T	XP_011541269.1:n.1202-1386A>T
XM_011542963.3:c.4256-1386A>T	XP_011541265.1:n.4256-1386A>T
XM_011542965.3:c.2831-1386A>T	XP_011541267.1:n.2831-1386A>T
XM_011542967.3:c.1202-1386A>T	XP_011541269.1:n.1202-1386A>T
XM_017018169.2:c.4058-1386A>T	XP_016873658.1:n.4058-1386A>T
XM_017018170.2:c.3845-1386A>T	XP_016873659.1:n.3845-1386A>T
XM_017018171.1:c.4370-1386A>T	XP_016873660.1:n.4370-1386A>T
XM_017018172.2:c.1730-1386A>T	XP_016873661.1:n.1730-1386A>T
NM_003105.6:c.4370-1386A>T MANE Select	NP_003096.2:n.4370-1386A>T