Canonical Allele Identifier: CA2004947504
Gene: SORL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.121577362A= , CM000673.2:g.121577362A= GRCh38
NC_000011.9:g.121448071A= , CM000673.1:g.121448071A= GRCh37
NC_000011.8:g.120953281A= NCBI36
NG_023313.1:g.130111A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260197.12:c.3542A= MANE Select ENSP00000260197.6:p.Asn1181=
ENST00000260197.11:c.3542A= ENSP00000260197.6:p.Asn1181=
ENST00000525532.5:c.374A= ENSP00000434634.1:p.Asn125=
ENST00000532694.5:c.80A= ENSP00000432131.1:p.Asn27=
ENST00000534286.5:c.272A= ENSP00000436447.1:p.Asn91=
NM_003105.5:c.3542A= NP_003096.1:p.Asn1181=
XM_011542963.1:c.3428A= XP_011541265.1:p.Asn1143=
XM_011542964.1:c.3542A= XP_011541266.1:p.Asn1181=
XM_011542965.1:c.2003A= XP_011541267.1:p.Asn668=
XM_011542966.1:c.902A= XP_011541268.1:p.Asn301=
XM_011542967.1:c.374A= XP_011541269.1:p.Asn125=
XM_011542963.3:c.3428A= XP_011541265.1:p.Asn1143=
XM_011542965.3:c.2003A= XP_011541267.1:p.Asn668=
XM_011542967.3:c.374A= XP_011541269.1:p.Asn125=
XM_017018169.2:c.3230A= XP_016873658.1:p.Asn1077=
XM_017018170.2:c.3017A= XP_016873659.1:p.Asn1006=
XM_017018171.1:c.3542A= XP_016873660.1:p.Asn1181=
XM_017018172.2:c.902A= XP_016873661.1:p.Asn301=
NM_003105.6:c.3542A= MANE Select NP_003096.2:p.Asn1181=