Canonical Allele Identifier: CA477218999

Gene: SORL1

Linked Data

• gnomAD v4: 11-121558822-C-T
• MyVariant Identifiers: chr11:g.121429531C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.121558822C>T , CM000673.2:g.121558822C>T	GRCh38
NC_000011.9:g.121429531C>T , CM000673.1:g.121429531C>T	GRCh37
NC_000011.8:g.120934741C>T	NCBI36
NG_023313.1:g.111571C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260197.12:c.2895C>T MANE Select	ENSP00000260197.6:p.Ala965=
ENST00000260197.11:c.2895C>T	ENSP00000260197.6:p.Ala965=
ENST00000529445.1:n.601C>T
NM_003105.5:c.2895C>T	NP_003096.1:p.Ala965=
XM_011542963.1:c.2895C>T	XP_011541265.1:p.Ala965=
XM_011542964.1:c.2895C>T	XP_011541266.1:p.Ala965=
XM_011542965.1:c.1356C>T	XP_011541267.1:p.Ala452=
XM_011542966.1:c.255C>T	XP_011541268.1:p.Ala85=
XM_011542963.3:c.2895C>T	XP_011541265.1:p.Ala965=
XM_011542965.3:c.1356C>T	XP_011541267.1:p.Ala452=
XM_017018169.2:c.2583C>T	XP_016873658.1:p.Ala861=
XM_017018170.2:c.2370C>T	XP_016873659.1:p.Ala790=
XM_017018171.1:c.2895C>T	XP_016873660.1:p.Ala965=
XM_017018172.2:c.255C>T	XP_016873661.1:p.Ala85=
NM_003105.6:c.2895C>T MANE Select	NP_003096.2:p.Ala965=