Canonical Allele Identifier: CA2004922123
Gene: SORL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.121605130A= , CM000673.2:g.121605130A= GRCh38
NC_000011.9:g.121475839A= , CM000673.1:g.121475839A= GRCh37
NC_000011.8:g.120981049A= NCBI36
NG_023313.1:g.157879A=

Transcript Alleles

HGVS Amino-acid change
ENST00000260197.12:c.4669A= MANE Select ENSP00000260197.6:p.Lys1557=
ENST00000260197.11:c.4669A= ENSP00000260197.6:p.Lys1557=
ENST00000525532.5:c.1501A= ENSP00000434634.1:p.Lys501=
ENST00000527934.1:c.514A= ENSP00000435405.1:p.Lys172=
ENST00000532694.5:c.1207A= ENSP00000432131.1:p.Lys403=
ENST00000534286.5:c.1399A= ENSP00000436447.1:p.Lys467=
NM_003105.5:c.4669A= NP_003096.1:p.Lys1557=
XM_011542963.1:c.4555A= XP_011541265.1:p.Lys1519=
XM_011542964.1:c.4669A= XP_011541266.1:p.Lys1557=
XM_011542965.1:c.3130A= XP_011541267.1:p.Lys1044=
XM_011542966.1:c.2029A= XP_011541268.1:p.Lys677=
XM_011542967.1:c.1501A= XP_011541269.1:p.Lys501=
XM_011542963.3:c.4555A= XP_011541265.1:p.Lys1519=
XM_011542965.3:c.3130A= XP_011541267.1:p.Lys1044=
XM_011542967.3:c.1501A= XP_011541269.1:p.Lys501=
XM_017018169.2:c.4357A= XP_016873658.1:p.Lys1453=
XM_017018170.2:c.4144A= XP_016873659.1:p.Lys1382=
XM_017018171.1:c.4669A= XP_016873660.1:p.Lys1557=
XM_017018172.2:c.2029A= XP_016873661.1:p.Lys677=
NM_003105.6:c.4669A= MANE Select NP_003096.2:p.Lys1557=