Canonical Allele Identifier: CA942945679

Gene: SORL1

Linked Data

• gnomAD v3: 11-121486496-TTG-T
• gnomAD v4: 11-121486496-TTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.121486497_121486498del , CM000673.2:g.121486497_121486498del	GRCh38
NC_000011.9:g.121357206_121357207del , CM000673.1:g.121357206_121357207del	GRCh37
NC_000011.8:g.120862416_120862417del	NCBI36
NG_023313.1:g.39246_39247del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260197.12:c.529-1535_529-1534del MANE Select	ENSP00000260197.6:n.529-1535_529-1534del
ENST00000260197.11:c.529-1535_529-1534del	ENSP00000260197.6:n.529-1535_529-1534del
ENST00000532451.1:n.481-1535_481-1534del
NM_003105.5:c.529-1535_529-1534del	NP_003096.1:n.529-1535_529-1534del
XM_011542963.1:c.529-1535_529-1534del	XP_011541265.1:n.529-1535_529-1534del
XM_011542964.1:c.529-1535_529-1534del	XP_011541266.1:n.529-1535_529-1534del
XM_011542963.3:c.529-1535_529-1534del	XP_011541265.1:n.529-1535_529-1534del
XM_017018169.2:c.217-1535_217-1534del	XP_016873658.1:n.217-1535_217-1534del
XM_017018170.2:c.3+40_3+41del	XP_016873659.1:n.3+40_3+41del
XM_017018171.1:c.529-1535_529-1534del	XP_016873660.1:n.529-1535_529-1534del
NM_003105.6:c.529-1535_529-1534del MANE Select	NP_003096.2:n.529-1535_529-1534del