LDH info

Canonical Allele Identifier: CA369856088
Gene: KCNH2 HGNC NCBI

Identifiers and link-outs to other resources

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150950228A>C , CM000669.2:g.150950228A>C GRCh38
NC_000007.13:g.150647316A>C , CM000669.1:g.150647316A>C GRCh37
NC_000007.12:g.150278249A>C NCBI36
NG_008916.1:g.32699T>G , LRG_288:g.32699T>G

Transcript Alleles

HGVS Amino-acid change
NM_000238.3:c.2338T>G , LRG_288t1:c.2338T>G NP_000229.1:p.Tyr780Asp
NM_001204798.1:c.1318T>G VV NP_001191727.1:p.Tyr440Asp
NM_172056.2:c.2338T>G , LRG_288t2:c.2338T>G NP_742053.1:p.Tyr780Asp
NM_172057.2:c.1318T>G , LRG_288t3:c.1318T>G NP_742054.1:p.Tyr440Asp
XM_011516185.1:c.2038T>G XP_011514487.1:p.Tyr680Asp
XM_011516186.1:c.2338T>G XP_011514488.1:p.Tyr780Asp
XM_011516185.2:c.2038T>G XP_011514487.1:p.Tyr680Asp
XM_011516186.3:c.2338T>G XP_011514488.1:p.Tyr780Asp
XM_017012195.1:c.2188T>G XP_016867684.1:p.Tyr730Asp
XM_017012196.1:c.2161T>G XP_016867685.1:p.Tyr721Asp
NM_000238.4:c.2338T>G VV MANE Preferred NP_000229.1:p.Tyr780Asp
NM_001204798.2:c.1318T>G VV NP_001191727.1:p.Tyr440Asp
ENST00000262186.9:c.2338T>G ENSP00000262186.5:p.Tyr780Asp
ENST00000330883.8:c.1318T>G ENSP00000328531.4:p.Tyr440Asp
ENST00000430723.4:c.1990T>G ENSP00000387657.4:p.Tyr664Asp
ENST00000461280.1:n.1625T>G
ENST00000473610.5:n.1970T>G
ENST00000532957.5:n.2561T>G