LDH info

Canonical Allele Identifier: CA11908201
Gene: SPP1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10516799

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87982041C>G , CM000666.2:g.87982041C>G GRCh38
NC_000004.11:g.88903193C>G , CM000666.1:g.88903193C>G GRCh37
NC_000004.10:g.89122217C>G NCBI36
NG_030362.1:g.11392C>G

Transcript Alleles

HGVS Amino-acid change
NM_000582.2:c.498+243C>G VV NP_000573.1:p.=
NM_001040058.1:c.540+243C>G VV NP_001035147.1:p.=
NM_001040060.1:c.459+243C>G VV NP_001035149.1:p.=
NM_001251829.1:c.417+243C>G VV NP_001238758.1:p.=
NM_001251830.1:c.579+243C>G VV NP_001238759.1:p.=
NM_001040058.2:c.540+243C>G VV MANE Preferred NP_001035147.1:p.=
ENST00000237623.11:c.498+243C>G ENSP00000237623.7:p.=
ENST00000360804.4:c.459+243C>G ENSP00000354042.4:p.=
ENST00000395080.7:c.540+243C>G ENSP00000378517.3:p.=
ENST00000508233.5:c.417+243C>G ENSP00000422973.1:p.=
ENST00000509659.5:n.829+243C>G
ENST00000614857.4:c.474+243C>G ENSP00000477824.1:p.=