Canonical Allele Identifier: CA2004886775
Gene: SORL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.121490207_121490208delinsCA , CM000673.2:g.121490207_121490208delinsCA GRCh38
NC_000011.9:g.121360916_121360917delinsCA , CM000673.1:g.121360916_121360917delinsCA GRCh37
NC_000011.8:g.120866126_120866127delinsCA NCBI36
NG_023313.1:g.42956_42957delinsCA

Transcript Alleles

HGVS Amino-acid change
ENST00000260197.12:c.758+97_758+98delinsCA MANE Select ENSP00000260197.6:n.758+97_758+98delinsCA...
ENST00000260197.11:c.758+97_758+98delinsCA ENSP00000260197.6:n.758+97_758+98delinsCA...
ENST00000532451.1:n.710+97_710+98delinsCA
NM_003105.5:c.758+97_758+98delinsCA NP_003096.1:n.758+97_758+98delinsCA
XM_011542963.1:c.758+97_758+98delinsCA XP_011541265.1:n.758+97_758+98delinsCA
XM_011542964.1:c.758+97_758+98delinsCA XP_011541266.1:n.758+97_758+98delinsCA
XM_011542963.3:c.758+97_758+98delinsCA XP_011541265.1:n.758+97_758+98delinsCA
XM_017018169.2:c.446+97_446+98delinsCA XP_016873658.1:n.446+97_446+98delinsCA
XM_017018170.2:c.233+97_233+98delinsCA XP_016873659.1:n.233+97_233+98delinsCA
XM_017018171.1:c.758+97_758+98delinsCA XP_016873660.1:n.758+97_758+98delinsCA
NM_003105.6:c.758+97_758+98delinsCA MANE Select NP_003096.2:n.758+97_758+98delinsCA