LDH info

Canonical Allele Identifier: CA13431351
Gene: SORL1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1784933

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.121618707G>A , CM000673.2:g.121618707G>A GRCh38
NC_000011.9:g.121489416G>A , CM000673.1:g.121489416G>A GRCh37
NC_000011.8:g.120994626G>A NCBI36
NG_023313.1:g.171456G>A

Transcript Alleles

HGVS Amino-acid change
NM_003105.5:c.5605-67G>A VV NP_003096.1:p.=
XM_011542963.1:c.5491-67G>A XP_011541265.1:p.=
XM_011542965.1:c.4066-67G>A XP_011541267.1:p.=
XM_011542966.1:c.2965-67G>A XP_011541268.1:p.=
XM_011542967.1:c.2437-67G>A XP_011541269.1:p.=
XM_011542963.3:c.5491-67G>A XP_011541265.1:p.=
XM_011542965.3:c.4066-67G>A XP_011541267.1:p.=
XM_011542967.3:c.2437-67G>A XP_011541269.1:p.=
XM_017018169.2:c.5293-67G>A XP_016873658.1:p.=
XM_017018170.2:c.5080-67G>A XP_016873659.1:p.=
XM_017018172.2:c.2965-67G>A XP_016873661.1:p.=
NM_003105.6:c.5605-67G>A VV MANE Preferred NP_003096.2:p.=
ENST00000260197.11:c.5605-67G>A ENSP00000260197.6:p.=
ENST00000524633.1:n.771-67G>A
ENST00000525532.5:c.2437-67G>A ENSP00000434634.1:p.=
ENST00000527934.1:c.1450-67G>A ENSP00000435405.1:p.=
ENST00000528339.5:n.3242-67G>A
ENST00000532694.5:c.2143-67G>A ENSP00000432131.1:p.=
ENST00000534286.5:c.2335-67G>A ENSP00000436447.1:p.=
ENST00000534754.5:n.1767-67G>A