Canonical Allele Identifier: CA2004919362
Gene: SORL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.121558774T= , CM000673.2:g.121558774T= GRCh38
NC_000011.9:g.121429483T= , CM000673.1:g.121429483T= GRCh37
NC_000011.8:g.120934693T= NCBI36
NG_023313.1:g.111523T=

Transcript Alleles

HGVS Amino-acid change
ENST00000260197.12:c.2847T= MANE Select ENSP00000260197.6:p.Ser949=
ENST00000260197.11:c.2847T= ENSP00000260197.6:p.Ser949=
ENST00000529445.1:n.553T=
NM_003105.5:c.2847T= NP_003096.1:p.Ser949=
XM_011542963.1:c.2847T= XP_011541265.1:p.Ser949=
XM_011542964.1:c.2847T= XP_011541266.1:p.Ser949=
XM_011542965.1:c.1308T= XP_011541267.1:p.Ser436=
XM_011542966.1:c.207T= XP_011541268.1:p.Ser69=
XM_011542963.3:c.2847T= XP_011541265.1:p.Ser949=
XM_011542965.3:c.1308T= XP_011541267.1:p.Ser436=
XM_017018169.2:c.2535T= XP_016873658.1:p.Ser845=
XM_017018170.2:c.2322T= XP_016873659.1:p.Ser774=
XM_017018171.1:c.2847T= XP_016873660.1:p.Ser949=
XM_017018172.2:c.207T= XP_016873661.1:p.Ser69=
NM_003105.6:c.2847T= MANE Select NP_003096.2:p.Ser949=