Canonical Allele Identifier: CA2793898617
Gene: SORL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.121604926G>A , CM000673.2:g.121604926G>A GRCh38
NC_000011.9:g.121475635G>A , CM000673.1:g.121475635G>A GRCh37
NC_000011.8:g.120980845G>A NCBI36
NG_023313.1:g.157675G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000260197.12:c.4652-187G>A MANE Select ENSP00000260197.6:n.4652-187G>A
ENST00000260197.11:c.4652-187G>A ENSP00000260197.6:n.4652-187G>A
ENST00000525532.5:c.1484-187G>A ENSP00000434634.1:n.1484-187G>A
ENST00000527934.1:c.497-187G>A ENSP00000435405.1:n.497-187G>A
ENST00000532694.5:c.1190-187G>A ENSP00000432131.1:n.1190-187G>A
ENST00000534286.5:c.1382-187G>A ENSP00000436447.1:n.1382-187G>A
NM_003105.5:c.4652-187G>A NP_003096.1:n.4652-187G>A
XM_011542963.1:c.4538-187G>A XP_011541265.1:n.4538-187G>A
XM_011542964.1:c.4652-187G>A XP_011541266.1:n.4652-187G>A
XM_011542965.1:c.3113-187G>A XP_011541267.1:n.3113-187G>A
XM_011542966.1:c.2012-187G>A XP_011541268.1:n.2012-187G>A
XM_011542967.1:c.1484-187G>A XP_011541269.1:n.1484-187G>A
XM_011542963.3:c.4538-187G>A XP_011541265.1:n.4538-187G>A
XM_011542965.3:c.3113-187G>A XP_011541267.1:n.3113-187G>A
XM_011542967.3:c.1484-187G>A XP_011541269.1:n.1484-187G>A
XM_017018169.2:c.4340-187G>A XP_016873658.1:n.4340-187G>A
XM_017018170.2:c.4127-187G>A XP_016873659.1:n.4127-187G>A
XM_017018171.1:c.4652-187G>A XP_016873660.1:n.4652-187G>A
XM_017018172.2:c.2012-187G>A XP_016873661.1:n.2012-187G>A
NM_003105.6:c.4652-187G>A MANE Select NP_003096.2:n.4652-187G>A