Canonical Allele Identifier: CA477218979

Gene: SORL1

Linked Data

• MyVariant Identifiers: chr11:g.121429501C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.121558792C>G , CM000673.2:g.121558792C>G	GRCh38
NC_000011.9:g.121429501C>G , CM000673.1:g.121429501C>G	GRCh37
NC_000011.8:g.120934711C>G	NCBI36
NG_023313.1:g.111541C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260197.12:c.2865C>G MANE Select	ENSP00000260197.6:p.Val955=
ENST00000260197.11:c.2865C>G	ENSP00000260197.6:p.Val955=
ENST00000529445.1:n.571C>G
NM_003105.5:c.2865C>G	NP_003096.1:p.Val955=
XM_011542963.1:c.2865C>G	XP_011541265.1:p.Val955=
XM_011542964.1:c.2865C>G	XP_011541266.1:p.Val955=
XM_011542965.1:c.1326C>G	XP_011541267.1:p.Val442=
XM_011542966.1:c.225C>G	XP_011541268.1:p.Val75=
XM_011542963.3:c.2865C>G	XP_011541265.1:p.Val955=
XM_011542965.3:c.1326C>G	XP_011541267.1:p.Val442=
XM_017018169.2:c.2553C>G	XP_016873658.1:p.Val851=
XM_017018170.2:c.2340C>G	XP_016873659.1:p.Val780=
XM_017018171.1:c.2865C>G	XP_016873660.1:p.Val955=
XM_017018172.2:c.225C>G	XP_016873661.1:p.Val75=
NM_003105.6:c.2865C>G MANE Select	NP_003096.2:p.Val955=