LDH info

Canonical Allele Identifier: CA369856094
Gene: KCNH2 HGNC NCBI

Identifiers and link-outs to other resources

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150950231G>C , CM000669.2:g.150950231G>C GRCh38
NC_000007.13:g.150647319G>C , CM000669.1:g.150647319G>C GRCh37
NC_000007.12:g.150278252G>C NCBI36
NG_008916.1:g.32696C>G , LRG_288:g.32696C>G

Transcript Alleles

HGVS Amino-acid change
NM_000238.3:c.2335C>G , LRG_288t1:c.2335C>G NP_000229.1:p.Leu779Val
NM_001204798.1:c.1315C>G VV NP_001191727.1:p.Leu439Val
NM_172056.2:c.2335C>G , LRG_288t2:c.2335C>G NP_742053.1:p.Leu779Val
NM_172057.2:c.1315C>G , LRG_288t3:c.1315C>G NP_742054.1:p.Leu439Val
XM_011516185.1:c.2035C>G XP_011514487.1:p.Leu679Val
XM_011516186.1:c.2335C>G XP_011514488.1:p.Leu779Val
XM_011516185.2:c.2035C>G XP_011514487.1:p.Leu679Val
XM_011516186.3:c.2335C>G XP_011514488.1:p.Leu779Val
XM_017012195.1:c.2185C>G XP_016867684.1:p.Leu729Val
XM_017012196.1:c.2158C>G XP_016867685.1:p.Leu720Val
NM_000238.4:c.2335C>G VV MANE Preferred NP_000229.1:p.Leu779Val
NM_001204798.2:c.1315C>G VV NP_001191727.1:p.Leu439Val
ENST00000262186.9:c.2335C>G ENSP00000262186.5:p.Leu779Val
ENST00000330883.8:c.1315C>G ENSP00000328531.4:p.Leu439Val
ENST00000430723.4:c.1987C>G ENSP00000387657.4:p.Leu663Val
ENST00000461280.1:n.1622C>G
ENST00000473610.5:n.1967C>G
ENST00000532957.5:n.2558C>G