Canonical Allele Identifier: CA477218100
Gene: SORL1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.121393375G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.121522666G>C , CM000673.2:g.121522666G>C GRCh38
NC_000011.9:g.121393375G>C , CM000673.1:g.121393375G>C GRCh37
NC_000011.8:g.120898585G>C NCBI36
NG_023313.1:g.75415G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000260197.12:c.1485G>C MANE Select ENSP00000260197.6:p.Leu495=
ENST00000260197.11:c.1485G>C ENSP00000260197.6:p.Leu495=
ENST00000532451.1:n.1437G>C
NM_003105.5:c.1485G>C NP_003096.1:p.Leu495=
XM_011542963.1:c.1485G>C XP_011541265.1:p.Leu495=
XM_011542964.1:c.1485G>C XP_011541266.1:p.Leu495=
XM_011542965.1:c.-138G>C XP_011541267.1:n.-138G>C
XM_011542963.3:c.1485G>C XP_011541265.1:p.Leu495=
XM_011542965.3:c.-138G>C XP_011541267.1:n.-138G>C
XM_017018169.2:c.1173G>C XP_016873658.1:p.Leu391=
XM_017018170.2:c.960G>C XP_016873659.1:p.Leu320=
XM_017018171.1:c.1485G>C XP_016873660.1:p.Leu495=
NM_003105.6:c.1485G>C MANE Select NP_003096.2:p.Leu495=