Canonical Allele Identifier: CA383036087

Gene: SORL1

Linked Data

• MyVariant Identifiers: chr11:g.121429490C>A (hg19) ; chr11:g.121558781C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.121558781C>A , CM000673.2:g.121558781C>A	GRCh38
NC_000011.9:g.121429490C>A , CM000673.1:g.121429490C>A	GRCh37
NC_000011.8:g.120934700C>A	NCBI36
NG_023313.1:g.111530C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000260197.12:c.2854C>A MANE Select	ENSP00000260197.6:p.Gln952Lys
ENST00000260197.11:c.2854C>A	ENSP00000260197.6:p.Gln952Lys
ENST00000529445.1:n.560C>A
NM_003105.5:c.2854C>A	NP_003096.1:p.Gln952Lys
XM_011542963.1:c.2854C>A	XP_011541265.1:p.Gln952Lys
XM_011542964.1:c.2854C>A	XP_011541266.1:p.Gln952Lys
XM_011542965.1:c.1315C>A	XP_011541267.1:p.Gln439Lys
XM_011542966.1:c.214C>A	XP_011541268.1:p.Gln72Lys
XM_011542963.3:c.2854C>A	XP_011541265.1:p.Gln952Lys
XM_011542965.3:c.1315C>A	XP_011541267.1:p.Gln439Lys
XM_017018169.2:c.2542C>A	XP_016873658.1:p.Gln848Lys
XM_017018170.2:c.2329C>A	XP_016873659.1:p.Gln777Lys
XM_017018171.1:c.2854C>A	XP_016873660.1:p.Gln952Lys
XM_017018172.2:c.214C>A	XP_016873661.1:p.Gln72Lys
NM_003105.6:c.2854C>A MANE Select	NP_003096.2:p.Gln952Lys