Canonical Allele Identifier: CA477218153

Gene: SORL1

Linked Data

• MyVariant Identifiers: chr11:g.121393668C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.121522959C>T , CM000673.2:g.121522959C>T	GRCh38
NC_000011.9:g.121393668C>T , CM000673.1:g.121393668C>T	GRCh37
NC_000011.8:g.120898878C>T	NCBI36
NG_023313.1:g.75708C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260197.12:c.1566C>T MANE Select	ENSP00000260197.6:p.Ile522=
ENST00000260197.11:c.1566C>T	ENSP00000260197.6:p.Ile522=
ENST00000532451.1:n.1518C>T
NM_003105.5:c.1566C>T	NP_003096.1:p.Ile522=
XM_011542963.1:c.1566C>T	XP_011541265.1:p.Ile522=
XM_011542964.1:c.1566C>T	XP_011541266.1:p.Ile522=
XM_011542965.1:c.-57C>T	XP_011541267.1:n.-57C>T
XM_011542963.3:c.1566C>T	XP_011541265.1:p.Ile522=
XM_011542965.3:c.-57C>T	XP_011541267.1:n.-57C>T
XM_017018169.2:c.1254C>T	XP_016873658.1:p.Ile418=
XM_017018170.2:c.1041C>T	XP_016873659.1:p.Ile347=
XM_017018171.1:c.1566C>T	XP_016873660.1:p.Ile522=
NM_003105.6:c.1566C>T MANE Select	NP_003096.2:p.Ile522=