Canonical Allele Identifier: CA2004922000
Gene: SORL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.121605024G= , CM000673.2:g.121605024G= GRCh38
NC_000011.9:g.121475733G= , CM000673.1:g.121475733G= GRCh37
NC_000011.8:g.120980943G= NCBI36
NG_023313.1:g.157773G=

Transcript Alleles

HGVS Amino-acid change
ENST00000260197.12:c.4652-89G= MANE Select ENSP00000260197.6:n.4652-89G=
ENST00000260197.11:c.4652-89G= ENSP00000260197.6:n.4652-89G=
ENST00000525532.5:c.1484-89G= ENSP00000434634.1:n.1484-89G=
ENST00000527934.1:c.497-89G= ENSP00000435405.1:n.497-89G=
ENST00000532694.5:c.1190-89G= ENSP00000432131.1:n.1190-89G=
ENST00000534286.5:c.1382-89G= ENSP00000436447.1:n.1382-89G=
NM_003105.5:c.4652-89G= NP_003096.1:n.4652-89G=
XM_011542963.1:c.4538-89G= XP_011541265.1:n.4538-89G=
XM_011542964.1:c.4652-89G= XP_011541266.1:n.4652-89G=
XM_011542965.1:c.3113-89G= XP_011541267.1:n.3113-89G=
XM_011542966.1:c.2012-89G= XP_011541268.1:n.2012-89G=
XM_011542967.1:c.1484-89G= XP_011541269.1:n.1484-89G=
XM_011542963.3:c.4538-89G= XP_011541265.1:n.4538-89G=
XM_011542965.3:c.3113-89G= XP_011541267.1:n.3113-89G=
XM_011542967.3:c.1484-89G= XP_011541269.1:n.1484-89G=
XM_017018169.2:c.4340-89G= XP_016873658.1:n.4340-89G=
XM_017018170.2:c.4127-89G= XP_016873659.1:n.4127-89G=
XM_017018171.1:c.4652-89G= XP_016873660.1:n.4652-89G=
XM_017018172.2:c.2012-89G= XP_016873661.1:n.2012-89G=
NM_003105.6:c.4652-89G= MANE Select NP_003096.2:n.4652-89G=