Canonical Allele Identifier: CA2004896319
Gene: SORL1 HGNC NCBI

Linked Data

dbSNP Id: rs1861769707

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.121505196T>C , CM000673.2:g.121505196T>C GRCh38
NC_000011.9:g.121375905T>C , CM000673.1:g.121375905T>C GRCh37
NC_000011.8:g.120881115T>C NCBI36
NG_023313.1:g.57945T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000260197.12:c.940-7807T>C MANE Select ENSP00000260197.6:n.940-7807T>C
ENST00000260197.11:c.940-7807T>C ENSP00000260197.6:n.940-7807T>C
ENST00000532451.1:n.892-7807T>C
NM_003105.5:c.940-7807T>C NP_003096.1:n.940-7807T>C
XM_011542963.1:c.940-7807T>C XP_011541265.1:n.940-7807T>C
XM_011542964.1:c.940-7807T>C XP_011541266.1:n.940-7807T>C
XM_011542963.3:c.940-7807T>C XP_011541265.1:n.940-7807T>C
XM_011542965.3:c.-683-7807T>C XP_011541267.1:n.-683-7807T>C
XM_017018169.2:c.628-7807T>C XP_016873658.1:n.628-7807T>C
XM_017018170.2:c.415-7807T>C XP_016873659.1:n.415-7807T>C
XM_017018171.1:c.940-7807T>C XP_016873660.1:n.940-7807T>C
NM_003105.6:c.940-7807T>C MANE Select NP_003096.2:n.940-7807T>C