Canonical Allele Identifier: CA383038380

Gene: SORL1

Linked Data

• MyVariant Identifiers: chr11:g.121475825A>T (hg19) ; chr11:g.121605116A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.121605116A>T , CM000673.2:g.121605116A>T	GRCh38
NC_000011.9:g.121475825A>T , CM000673.1:g.121475825A>T	GRCh37
NC_000011.8:g.120981035A>T	NCBI36
NG_023313.1:g.157865A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000260197.12:c.4655A>T MANE Select	ENSP00000260197.6:p.Glu1552Val
ENST00000260197.11:c.4655A>T	ENSP00000260197.6:p.Glu1552Val
ENST00000525532.5:c.1487A>T	ENSP00000434634.1:p.Glu496Val
ENST00000527934.1:c.500A>T	ENSP00000435405.1:p.Glu167Val
ENST00000532694.5:c.1193A>T	ENSP00000432131.1:p.Glu398Val
ENST00000534286.5:c.1385A>T	ENSP00000436447.1:p.Glu462Val
NM_003105.5:c.4655A>T	NP_003096.1:p.Glu1552Val
XM_011542963.1:c.4541A>T	XP_011541265.1:p.Glu1514Val
XM_011542964.1:c.4655A>T	XP_011541266.1:p.Glu1552Val
XM_011542965.1:c.3116A>T	XP_011541267.1:p.Glu1039Val
XM_011542966.1:c.2015A>T	XP_011541268.1:p.Glu672Val
XM_011542967.1:c.1487A>T	XP_011541269.1:p.Glu496Val
XM_011542963.3:c.4541A>T	XP_011541265.1:p.Glu1514Val
XM_011542965.3:c.3116A>T	XP_011541267.1:p.Glu1039Val
XM_011542967.3:c.1487A>T	XP_011541269.1:p.Glu496Val
XM_017018169.2:c.4343A>T	XP_016873658.1:p.Glu1448Val
XM_017018170.2:c.4130A>T	XP_016873659.1:p.Glu1377Val
XM_017018171.1:c.4655A>T	XP_016873660.1:p.Glu1552Val
XM_017018172.2:c.2015A>T	XP_016873661.1:p.Glu672Val
NM_003105.6:c.4655A>T MANE Select	NP_003096.2:p.Glu1552Val