Canonical Allele Identifier: CA672601868

Gene: SORL1

Linked Data

• dbSNP Id: rs1353728911
• gnomAD v3: 11-121631071-C-T
• gnomAD v4: 11-121631071-C-T
• MyVariant Identifiers: chr11:g.121501780C>T (hg19) ; chr11:g.121631071C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.121631071C>T , CM000673.2:g.121631071C>T	GRCh38
NC_000011.9:g.121501780C>T , CM000673.1:g.121501780C>T	GRCh37
NC_000011.8:g.121006990C>T	NCBI36
NG_023313.1:g.183820C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000260197.12:c.*1508C>T MANE Select	ENSP00000260197.6:n.*1508C>T
ENST00000260197.11:c.*1508C>T	ENSP00000260197.6:n.*1508C>T
ENST00000530365.1:n.759-945C>T
NM_003105.5:c.*1508C>T	NP_003096.1:n.*1508C>T
XM_011542963.1:c.*1508C>T	XP_011541265.1:n.*1508C>T
XM_011542965.1:c.*1508C>T	XP_011541267.1:n.*1508C>T
XM_011542966.1:c.*1508C>T	XP_011541268.1:n.*1508C>T
XM_011542967.1:c.*1508C>T	XP_011541269.1:n.*1508C>T
XM_011542965.3:c.*1508C>T	XP_011541267.1:n.*1508C>T
XM_011542967.3:c.*1508C>T	XP_011541269.1:n.*1508C>T
XM_017018172.2:c.*1508C>T	XP_016873661.1:n.*1508C>T
NM_003105.6:c.*1508C>T MANE Select	NP_003096.2:n.*1508C>T