Canonical Allele Identifier: CA383024948

Gene: SORL1

Linked Data

• MyVariant Identifiers: chr11:g.121448091G>T (hg19) ; chr11:g.121577382G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.121577382G>T , CM000673.2:g.121577382G>T	GRCh38
NC_000011.9:g.121448091G>T , CM000673.1:g.121448091G>T	GRCh37
NC_000011.8:g.120953301G>T	NCBI36
NG_023313.1:g.130131G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260197.12:c.3562G>T MANE Select	ENSP00000260197.6:p.Asp1188Tyr
ENST00000260197.11:c.3562G>T	ENSP00000260197.6:p.Asp1188Tyr
ENST00000525532.5:c.394G>T	ENSP00000434634.1:p.Asp132Tyr
ENST00000532694.5:c.100G>T	ENSP00000432131.1:p.Asp34Tyr
ENST00000534286.5:c.292G>T	ENSP00000436447.1:p.Asp98Tyr
NM_003105.5:c.3562G>T	NP_003096.1:p.Asp1188Tyr
XM_011542963.1:c.3448G>T	XP_011541265.1:p.Asp1150Tyr
XM_011542964.1:c.3562G>T	XP_011541266.1:p.Asp1188Tyr
XM_011542965.1:c.2023G>T	XP_011541267.1:p.Asp675Tyr
XM_011542966.1:c.922G>T	XP_011541268.1:p.Asp308Tyr
XM_011542967.1:c.394G>T	XP_011541269.1:p.Asp132Tyr
XM_011542963.3:c.3448G>T	XP_011541265.1:p.Asp1150Tyr
XM_011542965.3:c.2023G>T	XP_011541267.1:p.Asp675Tyr
XM_011542967.3:c.394G>T	XP_011541269.1:p.Asp132Tyr
XM_017018169.2:c.3250G>T	XP_016873658.1:p.Asp1084Tyr
XM_017018170.2:c.3037G>T	XP_016873659.1:p.Asp1013Tyr
XM_017018171.1:c.3562G>T	XP_016873660.1:p.Asp1188Tyr
XM_017018172.2:c.922G>T	XP_016873661.1:p.Asp308Tyr
NM_003105.6:c.3562G>T MANE Select	NP_003096.2:p.Asp1188Tyr