Canonical Allele Identifier: CA383035608

Gene: SORL1

Linked Data

• MyVariant Identifiers: chr11:g.121429312G>C (hg19) ; chr11:g.121558603G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.121558603G>C , CM000673.2:g.121558603G>C	GRCh38
NC_000011.9:g.121429312G>C , CM000673.1:g.121429312G>C	GRCh37
NC_000011.8:g.120934522G>C	NCBI36
NG_023313.1:g.111352G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260197.12:c.2676G>C MANE Select	ENSP00000260197.6:p.Trp892Cys
ENST00000260197.11:c.2676G>C	ENSP00000260197.6:p.Trp892Cys
ENST00000524873.1:n.404G>C
ENST00000529445.1:n.382G>C
NM_003105.5:c.2676G>C	NP_003096.1:p.Trp892Cys
XM_011542963.1:c.2676G>C	XP_011541265.1:p.Trp892Cys
XM_011542964.1:c.2676G>C	XP_011541266.1:p.Trp892Cys
XM_011542965.1:c.1137G>C	XP_011541267.1:p.Trp379Cys
XM_011542966.1:c.36G>C	XP_011541268.1:p.Trp12Cys
XM_011542963.3:c.2676G>C	XP_011541265.1:p.Trp892Cys
XM_011542965.3:c.1137G>C	XP_011541267.1:p.Trp379Cys
XM_017018169.2:c.2364G>C	XP_016873658.1:p.Trp788Cys
XM_017018170.2:c.2151G>C	XP_016873659.1:p.Trp717Cys
XM_017018171.1:c.2676G>C	XP_016873660.1:p.Trp892Cys
XM_017018172.2:c.36G>C	XP_016873661.1:p.Trp12Cys
NM_003105.6:c.2676G>C MANE Select	NP_003096.2:p.Trp892Cys