Canonical Allele Identifier: CA2004922222
Gene: SORL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.121605235T= , CM000673.2:g.121605235T= GRCh38
NC_000011.9:g.121475944T= , CM000673.1:g.121475944T= GRCh37
NC_000011.8:g.120981154T= NCBI36
NG_023313.1:g.157984T=

Transcript Alleles

HGVS Amino-acid change
ENST00000260197.12:c.4774T= MANE Select ENSP00000260197.6:p.Tyr1592=
ENST00000260197.11:c.4774T= ENSP00000260197.6:p.Tyr1592=
ENST00000525532.5:c.1606T= ENSP00000434634.1:p.Tyr536=
ENST00000527934.1:c.619T= ENSP00000435405.1:p.Tyr207=
ENST00000532694.5:c.1312T= ENSP00000432131.1:p.Tyr438=
ENST00000534286.5:c.1504T= ENSP00000436447.1:p.Tyr502=
NM_003105.5:c.4774T= NP_003096.1:p.Tyr1592=
XM_011542963.1:c.4660T= XP_011541265.1:p.Tyr1554=
XM_011542964.1:c.4774T= XP_011541266.1:p.Tyr1592=
XM_011542965.1:c.3235T= XP_011541267.1:p.Tyr1079=
XM_011542966.1:c.2134T= XP_011541268.1:p.Tyr712=
XM_011542967.1:c.1606T= XP_011541269.1:p.Tyr536=
XM_011542963.3:c.4660T= XP_011541265.1:p.Tyr1554=
XM_011542965.3:c.3235T= XP_011541267.1:p.Tyr1079=
XM_011542967.3:c.1606T= XP_011541269.1:p.Tyr536=
XM_017018169.2:c.4462T= XP_016873658.1:p.Tyr1488=
XM_017018170.2:c.4249T= XP_016873659.1:p.Tyr1417=
XM_017018171.1:c.4774T= XP_016873660.1:p.Tyr1592=
XM_017018172.2:c.2134T= XP_016873661.1:p.Tyr712=
NM_003105.6:c.4774T= MANE Select NP_003096.2:p.Tyr1592=