Canonical Allele Identifier: CA383038898

Gene: SORL1

Linked Data

• MyVariant Identifiers: chr11:g.121475932T>G (hg19) ; chr11:g.121605223T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.121605223T>G , CM000673.2:g.121605223T>G	GRCh38
NC_000011.9:g.121475932T>G , CM000673.1:g.121475932T>G	GRCh37
NC_000011.8:g.120981142T>G	NCBI36
NG_023313.1:g.157972T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000260197.12:c.4762T>G MANE Select	ENSP00000260197.6:p.Tyr1588Asp
ENST00000260197.11:c.4762T>G	ENSP00000260197.6:p.Tyr1588Asp
ENST00000525532.5:c.1594T>G	ENSP00000434634.1:p.Tyr532Asp
ENST00000527934.1:c.607T>G	ENSP00000435405.1:p.Tyr203Asp
ENST00000532694.5:c.1300T>G	ENSP00000432131.1:p.Tyr434Asp
ENST00000534286.5:c.1492T>G	ENSP00000436447.1:p.Tyr498Asp
NM_003105.5:c.4762T>G	NP_003096.1:p.Tyr1588Asp
XM_011542963.1:c.4648T>G	XP_011541265.1:p.Tyr1550Asp
XM_011542964.1:c.4762T>G	XP_011541266.1:p.Tyr1588Asp
XM_011542965.1:c.3223T>G	XP_011541267.1:p.Tyr1075Asp
XM_011542966.1:c.2122T>G	XP_011541268.1:p.Tyr708Asp
XM_011542967.1:c.1594T>G	XP_011541269.1:p.Tyr532Asp
XM_011542963.3:c.4648T>G	XP_011541265.1:p.Tyr1550Asp
XM_011542965.3:c.3223T>G	XP_011541267.1:p.Tyr1075Asp
XM_011542967.3:c.1594T>G	XP_011541269.1:p.Tyr532Asp
XM_017018169.2:c.4450T>G	XP_016873658.1:p.Tyr1484Asp
XM_017018170.2:c.4237T>G	XP_016873659.1:p.Tyr1413Asp
XM_017018171.1:c.4762T>G	XP_016873660.1:p.Tyr1588Asp
XM_017018172.2:c.2122T>G	XP_016873661.1:p.Tyr708Asp
NM_003105.6:c.4762T>G MANE Select	NP_003096.2:p.Tyr1588Asp