Canonical Allele Identifier: CA2004883535
Gene: SORL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.121486479_121486480delinsTC , CM000673.2:g.121486479_121486480delinsTC GRCh38
NC_000011.9:g.121357188_121357189delinsTC , CM000673.1:g.121357188_121357189delinsTC GRCh37
NC_000011.8:g.120862398_120862399delinsTC NCBI36
NG_023313.1:g.39228_39229delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000260197.12:c.529-1553_529-1552delinsTC MANE Select ENSP00000260197.6:n.529-1553_529-1552delinsTC
ENST00000260197.11:c.529-1553_529-1552delinsTC ENSP00000260197.6:n.529-1553_529-1552delinsTC
ENST00000532451.1:n.481-1553_481-1552delinsTC
NM_003105.5:c.529-1553_529-1552delinsTC NP_003096.1:n.529-1553_529-1552delinsTC
XM_011542963.1:c.529-1553_529-1552delinsTC XP_011541265.1:n.529-1553_529-1552delinsTC
XM_011542964.1:c.529-1553_529-1552delinsTC XP_011541266.1:n.529-1553_529-1552delinsTC
XM_011542963.3:c.529-1553_529-1552delinsTC XP_011541265.1:n.529-1553_529-1552delinsTC
XM_017018169.2:c.217-1553_217-1552delinsTC XP_016873658.1:n.217-1553_217-1552delinsTC
XM_017018170.2:c.3+22_3+23delinsTC XP_016873659.1:n.3+22_3+23delinsTC
XM_017018171.1:c.529-1553_529-1552delinsTC XP_016873660.1:n.529-1553_529-1552delinsTC
NM_003105.6:c.529-1553_529-1552delinsTC MANE Select NP_003096.2:n.529-1553_529-1552delinsTC