LDH info

Canonical Allele Identifier: CA458871228
Gene: KCNH2 HGNC NCBI

Identifiers and link-outs to other resources

MyVariant Identifiers: chr7:g.150647314G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150950226G>A , CM000669.2:g.150950226G>A GRCh38
NC_000007.13:g.150647314G>A , CM000669.1:g.150647314G>A GRCh37
NC_000007.12:g.150278247G>A NCBI36
NG_008916.1:g.32701C>T , LRG_288:g.32701C>T

Transcript Alleles

HGVS Amino-acid change
NM_000238.3:c.2340C>T , LRG_288t1:c.2340C>T NP_000229.1:p.Tyr780=
NM_001204798.1:c.1320C>T VV NP_001191727.1:p.Tyr440=
NM_172056.2:c.2340C>T , LRG_288t2:c.2340C>T NP_742053.1:p.Tyr780=
NM_172057.2:c.1320C>T , LRG_288t3:c.1320C>T NP_742054.1:p.Tyr440=
XM_011516185.1:c.2040C>T XP_011514487.1:p.Tyr680=
XM_011516186.1:c.2340C>T XP_011514488.1:p.Tyr780=
XM_011516185.2:c.2040C>T XP_011514487.1:p.Tyr680=
XM_011516186.3:c.2340C>T XP_011514488.1:p.Tyr780=
XM_017012195.1:c.2190C>T XP_016867684.1:p.Tyr730=
XM_017012196.1:c.2163C>T XP_016867685.1:p.Tyr721=
NM_000238.4:c.2340C>T VV MANE Preferred NP_000229.1:p.Tyr780=
NM_001204798.2:c.1320C>T VV NP_001191727.1:p.Tyr440=
ENST00000262186.9:c.2340C>T ENSP00000262186.5:p.Tyr780=
ENST00000330883.8:c.1320C>T ENSP00000328531.4:p.Tyr440=
ENST00000430723.4:c.1992C>T ENSP00000387657.4:p.Tyr664=
ENST00000461280.1:n.1627C>T
ENST00000473610.5:n.1972C>T
ENST00000532957.5:n.2563C>T