Canonical Allele Identifier: CA477221656

Gene: SORL1

Linked Data

• MyVariant Identifiers: chr11:g.121475835G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.121605126G>T , CM000673.2:g.121605126G>T	GRCh38
NC_000011.9:g.121475835G>T , CM000673.1:g.121475835G>T	GRCh37
NC_000011.8:g.120981045G>T	NCBI36
NG_023313.1:g.157875G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260197.12:c.4665G>T MANE Select	ENSP00000260197.6:p.Val1555=
ENST00000260197.11:c.4665G>T	ENSP00000260197.6:p.Val1555=
ENST00000525532.5:c.1497G>T	ENSP00000434634.1:p.Val499=
ENST00000527934.1:c.510G>T	ENSP00000435405.1:p.Val170=
ENST00000532694.5:c.1203G>T	ENSP00000432131.1:p.Val401=
ENST00000534286.5:c.1395G>T	ENSP00000436447.1:p.Val465=
NM_003105.5:c.4665G>T	NP_003096.1:p.Val1555=
XM_011542963.1:c.4551G>T	XP_011541265.1:p.Val1517=
XM_011542964.1:c.4665G>T	XP_011541266.1:p.Val1555=
XM_011542965.1:c.3126G>T	XP_011541267.1:p.Val1042=
XM_011542966.1:c.2025G>T	XP_011541268.1:p.Val675=
XM_011542967.1:c.1497G>T	XP_011541269.1:p.Val499=
XM_011542963.3:c.4551G>T	XP_011541265.1:p.Val1517=
XM_011542965.3:c.3126G>T	XP_011541267.1:p.Val1042=
XM_011542967.3:c.1497G>T	XP_011541269.1:p.Val499=
XM_017018169.2:c.4353G>T	XP_016873658.1:p.Val1451=
XM_017018170.2:c.4140G>T	XP_016873659.1:p.Val1380=
XM_017018171.1:c.4665G>T	XP_016873660.1:p.Val1555=
XM_017018172.2:c.2025G>T	XP_016873661.1:p.Val675=
NM_003105.6:c.4665G>T MANE Select	NP_003096.2:p.Val1555=