Canonical Allele Identifier: CA229873655

Gene: SORL1

Linked Data

• dbSNP Id: rs1003960634
• MyVariant Identifiers: chr11:g.121475936A>G (hg19) ; chr11:g.121605227A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.121605227A>G , CM000673.2:g.121605227A>G	GRCh38
NC_000011.9:g.121475936A>G , CM000673.1:g.121475936A>G	GRCh37
NC_000011.8:g.120981146A>G	NCBI36
NG_023313.1:g.157976A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000260197.12:c.4766A>G MANE Select	ENSP00000260197.6:p.Asn1589Ser
ENST00000260197.11:c.4766A>G	ENSP00000260197.6:p.Asn1589Ser
ENST00000525532.5:c.1598A>G	ENSP00000434634.1:p.Asn533Ser
ENST00000527934.1:c.611A>G	ENSP00000435405.1:p.Asn204Ser
ENST00000532694.5:c.1304A>G	ENSP00000432131.1:p.Asn435Ser
ENST00000534286.5:c.1496A>G	ENSP00000436447.1:p.Asn499Ser
NM_003105.5:c.4766A>G	NP_003096.1:p.Asn1589Ser
XM_011542963.1:c.4652A>G	XP_011541265.1:p.Asn1551Ser
XM_011542964.1:c.4766A>G	XP_011541266.1:p.Asn1589Ser
XM_011542965.1:c.3227A>G	XP_011541267.1:p.Asn1076Ser
XM_011542966.1:c.2126A>G	XP_011541268.1:p.Asn709Ser
XM_011542967.1:c.1598A>G	XP_011541269.1:p.Asn533Ser
XM_011542963.3:c.4652A>G	XP_011541265.1:p.Asn1551Ser
XM_011542965.3:c.3227A>G	XP_011541267.1:p.Asn1076Ser
XM_011542967.3:c.1598A>G	XP_011541269.1:p.Asn533Ser
XM_017018169.2:c.4454A>G	XP_016873658.1:p.Asn1485Ser
XM_017018170.2:c.4241A>G	XP_016873659.1:p.Asn1414Ser
XM_017018171.1:c.4766A>G	XP_016873660.1:p.Asn1589Ser
XM_017018172.2:c.2126A>G	XP_016873661.1:p.Asn709Ser
NM_003105.6:c.4766A>G MANE Select	NP_003096.2:p.Asn1589Ser