LDH info

Canonical Allele Identifier: CA229853551
Gene: SORL1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs3781835

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.121577545G>A , CM000673.2:g.121577545G>A GRCh38
NC_000011.9:g.121448254G>A , CM000673.1:g.121448254G>A GRCh37
NC_000011.8:g.120953464G>A NCBI36
NG_023313.1:g.130294G>A

Transcript Alleles

HGVS Amino-acid change
NM_003105.5:c.3580+145G>A VV NP_003096.1:p.=
XM_011542963.1:c.3466+145G>A XP_011541265.1:p.=
XM_011542964.1:c.3580+145G>A XP_011541266.1:p.=
XM_011542965.1:c.2041+145G>A XP_011541267.1:p.=
XM_011542966.1:c.940+145G>A XP_011541268.1:p.=
XM_011542967.1:c.412+145G>A XP_011541269.1:p.=
XM_011542963.3:c.3466+145G>A XP_011541265.1:p.=
XM_011542965.3:c.2041+145G>A XP_011541267.1:p.=
XM_011542967.3:c.412+145G>A XP_011541269.1:p.=
XM_017018169.2:c.3268+145G>A XP_016873658.1:p.=
XM_017018170.2:c.3055+145G>A XP_016873659.1:p.=
XM_017018171.1:c.3580+145G>A XP_016873660.1:p.=
XM_017018172.2:c.940+145G>A XP_016873661.1:p.=
NM_003105.6:c.3580+145G>A VV MANE Preferred NP_003096.2:p.=
ENST00000260197.11:c.3580+145G>A ENSP00000260197.6:p.=
ENST00000525532.5:c.412+145G>A ENSP00000434634.1:p.=
ENST00000532694.5:c.118+145G>A ENSP00000432131.1:p.=
ENST00000534286.5:c.310+145G>A ENSP00000436447.1:p.=