Canonical Allele Identifier: CA477218129

Gene: SORL1

Linked Data

• MyVariant Identifiers: chr11:g.121393626C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.121522917C>T , CM000673.2:g.121522917C>T	GRCh38
NC_000011.9:g.121393626C>T , CM000673.1:g.121393626C>T	GRCh37
NC_000011.8:g.120898836C>T	NCBI36
NG_023313.1:g.75666C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000260197.12:c.1524C>T MANE Select	ENSP00000260197.6:p.Gly508=
ENST00000260197.11:c.1524C>T	ENSP00000260197.6:p.Gly508=
ENST00000532451.1:n.1476C>T
NM_003105.5:c.1524C>T	NP_003096.1:p.Gly508=
XM_011542963.1:c.1524C>T	XP_011541265.1:p.Gly508=
XM_011542964.1:c.1524C>T	XP_011541266.1:p.Gly508=
XM_011542965.1:c.-99C>T	XP_011541267.1:n.-99C>T
XM_011542963.3:c.1524C>T	XP_011541265.1:p.Gly508=
XM_011542965.3:c.-99C>T	XP_011541267.1:n.-99C>T
XM_017018169.2:c.1212C>T	XP_016873658.1:p.Gly404=
XM_017018170.2:c.999C>T	XP_016873659.1:p.Gly333=
XM_017018171.1:c.1524C>T	XP_016873660.1:p.Gly508=
NM_003105.6:c.1524C>T MANE Select	NP_003096.2:p.Gly508=