Canonical Allele Identifier: CA383038404

Gene: SORL1

Linked Data

• dbSNP Id: rs1565351908
• gnomAD v4: 11-121605128-A-G
• MyVariant Identifiers: chr11:g.121475837A>G (hg19) ; chr11:g.121605128A>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000260197.12:c.4667A>G MANE Select	ENSP00000260197.6:p.Tyr1556Cys
ENST00000260197.11:c.4667A>G	ENSP00000260197.6:p.Tyr1556Cys
ENST00000525532.5:c.1499A>G	ENSP00000434634.1:p.Tyr500Cys
ENST00000527934.1:c.512A>G	ENSP00000435405.1:p.Tyr171Cys
ENST00000532694.5:c.1205A>G	ENSP00000432131.1:p.Tyr402Cys
ENST00000534286.5:c.1397A>G	ENSP00000436447.1:p.Tyr466Cys
NM_003105.5:c.4667A>G	NP_003096.1:p.Tyr1556Cys
XM_011542963.1:c.4553A>G	XP_011541265.1:p.Tyr1518Cys
XM_011542964.1:c.4667A>G	XP_011541266.1:p.Tyr1556Cys
XM_011542965.1:c.3128A>G	XP_011541267.1:p.Tyr1043Cys
XM_011542966.1:c.2027A>G	XP_011541268.1:p.Tyr676Cys
XM_011542967.1:c.1499A>G	XP_011541269.1:p.Tyr500Cys
XM_011542963.3:c.4553A>G	XP_011541265.1:p.Tyr1518Cys
XM_011542965.3:c.3128A>G	XP_011541267.1:p.Tyr1043Cys
XM_011542967.3:c.1499A>G	XP_011541269.1:p.Tyr500Cys
XM_017018169.2:c.4355A>G	XP_016873658.1:p.Tyr1452Cys
XM_017018170.2:c.4142A>G	XP_016873659.1:p.Tyr1381Cys
XM_017018171.1:c.4667A>G	XP_016873660.1:p.Tyr1556Cys
XM_017018172.2:c.2027A>G	XP_016873661.1:p.Tyr676Cys
NM_003105.6:c.4667A>G MANE Select	NP_003096.2:p.Tyr1556Cys