Canonical Allele Identifier: CA383036153

Gene: SORL1

Linked Data

• MyVariant Identifiers: chr11:g.121429522C>G (hg19) ; chr11:g.121558813C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.121558813C>G , CM000673.2:g.121558813C>G	GRCh38
NC_000011.9:g.121429522C>G , CM000673.1:g.121429522C>G	GRCh37
NC_000011.8:g.120934732C>G	NCBI36
NG_023313.1:g.111562C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260197.12:c.2886C>G MANE Select	ENSP00000260197.6:p.His962Gln
ENST00000260197.11:c.2886C>G	ENSP00000260197.6:p.His962Gln
ENST00000529445.1:n.592C>G
NM_003105.5:c.2886C>G	NP_003096.1:p.His962Gln
XM_011542963.1:c.2886C>G	XP_011541265.1:p.His962Gln
XM_011542964.1:c.2886C>G	XP_011541266.1:p.His962Gln
XM_011542965.1:c.1347C>G	XP_011541267.1:p.His449Gln
XM_011542966.1:c.246C>G	XP_011541268.1:p.His82Gln
XM_011542963.3:c.2886C>G	XP_011541265.1:p.His962Gln
XM_011542965.3:c.1347C>G	XP_011541267.1:p.His449Gln
XM_017018169.2:c.2574C>G	XP_016873658.1:p.His858Gln
XM_017018170.2:c.2361C>G	XP_016873659.1:p.His787Gln
XM_017018171.1:c.2886C>G	XP_016873660.1:p.His962Gln
XM_017018172.2:c.246C>G	XP_016873661.1:p.His82Gln
NM_003105.6:c.2886C>G MANE Select	NP_003096.2:p.His962Gln