Canonical Allele Identifier: CA2004922216
Gene: SORL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.121605231C= , CM000673.2:g.121605231C= GRCh38
NC_000011.9:g.121475940C= , CM000673.1:g.121475940C= GRCh37
NC_000011.8:g.120981150C= NCBI36
NG_023313.1:g.157980C=

Transcript Alleles

HGVS Amino-acid change
ENST00000260197.12:c.4770C= MANE Select ENSP00000260197.6:p.Val1590=
ENST00000260197.11:c.4770C= ENSP00000260197.6:p.Val1590=
ENST00000525532.5:c.1602C= ENSP00000434634.1:p.Val534=
ENST00000527934.1:c.615C= ENSP00000435405.1:p.Val205=
ENST00000532694.5:c.1308C= ENSP00000432131.1:p.Val436=
ENST00000534286.5:c.1500C= ENSP00000436447.1:p.Val500=
NM_003105.5:c.4770C= NP_003096.1:p.Val1590=
XM_011542963.1:c.4656C= XP_011541265.1:p.Val1552=
XM_011542964.1:c.4770C= XP_011541266.1:p.Val1590=
XM_011542965.1:c.3231C= XP_011541267.1:p.Val1077=
XM_011542966.1:c.2130C= XP_011541268.1:p.Val710=
XM_011542967.1:c.1602C= XP_011541269.1:p.Val534=
XM_011542963.3:c.4656C= XP_011541265.1:p.Val1552=
XM_011542965.3:c.3231C= XP_011541267.1:p.Val1077=
XM_011542967.3:c.1602C= XP_011541269.1:p.Val534=
XM_017018169.2:c.4458C= XP_016873658.1:p.Val1486=
XM_017018170.2:c.4245C= XP_016873659.1:p.Val1415=
XM_017018171.1:c.4770C= XP_016873660.1:p.Val1590=
XM_017018172.2:c.2130C= XP_016873661.1:p.Val710=
NM_003105.6:c.4770C= MANE Select NP_003096.2:p.Val1590=