Canonical Allele Identifier: CA383038923

Gene: SORL1

Linked Data

• MyVariant Identifiers: chr11:g.121475942A>G (hg19) ; chr11:g.121605233A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.121605233A>G , CM000673.2:g.121605233A>G	GRCh38
NC_000011.9:g.121475942A>G , CM000673.1:g.121475942A>G	GRCh37
NC_000011.8:g.120981152A>G	NCBI36
NG_023313.1:g.157982A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260197.12:c.4772A>G MANE Select	ENSP00000260197.6:p.Tyr1591Cys
ENST00000260197.11:c.4772A>G	ENSP00000260197.6:p.Tyr1591Cys
ENST00000525532.5:c.1604A>G	ENSP00000434634.1:p.Tyr535Cys
ENST00000527934.1:c.617A>G	ENSP00000435405.1:p.Tyr206Cys
ENST00000532694.5:c.1310A>G	ENSP00000432131.1:p.Tyr437Cys
ENST00000534286.5:c.1502A>G	ENSP00000436447.1:p.Tyr501Cys
NM_003105.5:c.4772A>G	NP_003096.1:p.Tyr1591Cys
XM_011542963.1:c.4658A>G	XP_011541265.1:p.Tyr1553Cys
XM_011542964.1:c.4772A>G	XP_011541266.1:p.Tyr1591Cys
XM_011542965.1:c.3233A>G	XP_011541267.1:p.Tyr1078Cys
XM_011542966.1:c.2132A>G	XP_011541268.1:p.Tyr711Cys
XM_011542967.1:c.1604A>G	XP_011541269.1:p.Tyr535Cys
XM_011542963.3:c.4658A>G	XP_011541265.1:p.Tyr1553Cys
XM_011542965.3:c.3233A>G	XP_011541267.1:p.Tyr1078Cys
XM_011542967.3:c.1604A>G	XP_011541269.1:p.Tyr535Cys
XM_017018169.2:c.4460A>G	XP_016873658.1:p.Tyr1487Cys
XM_017018170.2:c.4247A>G	XP_016873659.1:p.Tyr1416Cys
XM_017018171.1:c.4772A>G	XP_016873660.1:p.Tyr1591Cys
XM_017018172.2:c.2132A>G	XP_016873661.1:p.Tyr711Cys
NM_003105.6:c.4772A>G MANE Select	NP_003096.2:p.Tyr1591Cys