Canonical Allele Identifier: CA383038405
Gene: SORL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.121605128A>T , CM000673.2:g.121605128A>T GRCh38
NC_000011.9:g.121475837A>T , CM000673.1:g.121475837A>T GRCh37
NC_000011.8:g.120981047A>T NCBI36
NG_023313.1:g.157877A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000260197.12:c.4667A>T MANE Select ENSP00000260197.6:p.Tyr1556Phe
ENST00000260197.11:c.4667A>T ENSP00000260197.6:p.Tyr1556Phe
ENST00000525532.5:c.1499A>T ENSP00000434634.1:p.Tyr500Phe
ENST00000527934.1:c.512A>T ENSP00000435405.1:p.Tyr171Phe
ENST00000532694.5:c.1205A>T ENSP00000432131.1:p.Tyr402Phe
ENST00000534286.5:c.1397A>T ENSP00000436447.1:p.Tyr466Phe
NM_003105.5:c.4667A>T NP_003096.1:p.Tyr1556Phe
XM_011542963.1:c.4553A>T XP_011541265.1:p.Tyr1518Phe
XM_011542964.1:c.4667A>T XP_011541266.1:p.Tyr1556Phe
XM_011542965.1:c.3128A>T XP_011541267.1:p.Tyr1043Phe
XM_011542966.1:c.2027A>T XP_011541268.1:p.Tyr676Phe
XM_011542967.1:c.1499A>T XP_011541269.1:p.Tyr500Phe
XM_011542963.3:c.4553A>T XP_011541265.1:p.Tyr1518Phe
XM_011542965.3:c.3128A>T XP_011541267.1:p.Tyr1043Phe
XM_011542967.3:c.1499A>T XP_011541269.1:p.Tyr500Phe
XM_017018169.2:c.4355A>T XP_016873658.1:p.Tyr1452Phe
XM_017018170.2:c.4142A>T XP_016873659.1:p.Tyr1381Phe
XM_017018171.1:c.4667A>T XP_016873660.1:p.Tyr1556Phe
XM_017018172.2:c.2027A>T XP_016873661.1:p.Tyr676Phe
NM_003105.6:c.4667A>T MANE Select NP_003096.2:p.Tyr1556Phe