Canonical Allele Identifier: CA477219514

Gene: SORL1

Linked Data

• MyVariant Identifiers: chr11:g.121456965C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.121586256C>A , CM000673.2:g.121586256C>A	GRCh38
NC_000011.9:g.121456965C>A , CM000673.1:g.121456965C>A	GRCh37
NC_000011.8:g.120962175C>A	NCBI36
NG_023313.1:g.139005C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000260197.12:c.3741C>A MANE Select	ENSP00000260197.6:p.Gly1247=
ENST00000260197.11:c.3741C>A	ENSP00000260197.6:p.Gly1247=
ENST00000525532.5:c.573C>A	ENSP00000434634.1:p.Gly191=
ENST00000532694.5:c.279C>A	ENSP00000432131.1:p.Gly93=
ENST00000534286.5:c.471C>A	ENSP00000436447.1:p.Gly157=
NM_003105.5:c.3741C>A	NP_003096.1:p.Gly1247=
XM_011542963.1:c.3627C>A	XP_011541265.1:p.Gly1209=
XM_011542964.1:c.3741C>A	XP_011541266.1:p.Gly1247=
XM_011542965.1:c.2202C>A	XP_011541267.1:p.Gly734=
XM_011542966.1:c.1101C>A	XP_011541268.1:p.Gly367=
XM_011542967.1:c.573C>A	XP_011541269.1:p.Gly191=
XM_011542963.3:c.3627C>A	XP_011541265.1:p.Gly1209=
XM_011542965.3:c.2202C>A	XP_011541267.1:p.Gly734=
XM_011542967.3:c.573C>A	XP_011541269.1:p.Gly191=
XM_017018169.2:c.3429C>A	XP_016873658.1:p.Gly1143=
XM_017018170.2:c.3216C>A	XP_016873659.1:p.Gly1072=
XM_017018171.1:c.3741C>A	XP_016873660.1:p.Gly1247=
XM_017018172.2:c.1101C>A	XP_016873661.1:p.Gly367=
NM_003105.6:c.3741C>A MANE Select	NP_003096.2:p.Gly1247=