Canonical Allele Identifier: CA229897462

Gene: SORL1

Linked Data

• dbSNP Id: rs763648936
• gnomAD v3: 11-121552983-A-T
• gnomAD v4: 11-121552983-A-T
• MyVariant Identifiers: chr11:g.121423692A>T (hg19) ; chr11:g.121552983A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.121552983A>T , CM000673.2:g.121552983A>T	GRCh38
NC_000011.9:g.121423692A>T , CM000673.1:g.121423692A>T	GRCh37
NC_000011.8:g.120928902A>T	NCBI36
NG_023313.1:g.105732A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000260197.12:c.2267-954A>T MANE Select	ENSP00000260197.6:n.2267-954A>T
ENST00000260197.11:c.2267-954A>T	ENSP00000260197.6:n.2267-954A>T
NM_003105.5:c.2267-954A>T	NP_003096.1:n.2267-954A>T
XM_011542963.1:c.2267-954A>T	XP_011541265.1:n.2267-954A>T
XM_011542964.1:c.2267-954A>T	XP_011541266.1:n.2267-954A>T
XM_011542965.1:c.728-954A>T	XP_011541267.1:n.728-954A>T
XM_011542963.3:c.2267-954A>T	XP_011541265.1:n.2267-954A>T
XM_011542965.3:c.728-954A>T	XP_011541267.1:n.728-954A>T
XM_017018169.2:c.1955-954A>T	XP_016873658.1:n.1955-954A>T
XM_017018170.2:c.1742-954A>T	XP_016873659.1:n.1742-954A>T
XM_017018171.1:c.2267-954A>T	XP_016873660.1:n.2267-954A>T
XM_017018172.2:c.-282-954A>T	XP_016873661.1:n.-282-954A>T
NM_003105.6:c.2267-954A>T MANE Select	NP_003096.2:n.2267-954A>T