LDH info

Canonical Allele Identifier: CA291012372
Gene: ACBD4 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1053578

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.45143918T>C , CM000679.2:g.45143918T>C GRCh38
NC_000017.10:g.43221285T>C , CM000679.1:g.43221285T>C GRCh37
NC_000017.9:g.40577068T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001135704.1:c.*277T>C VV NP_001129176.1:p.=
NM_001135705.1:c.*347T>C VV NP_001129177.1:p.=
NM_001135706.1:c.*277T>C VV NP_001129178.1:p.=
NM_024722.2:c.*347T>C VV NP_078998.1:p.=
XM_005257673.1:c.*277T>C XP_005257730.1:p.=
XM_005257674.1:c.*277T>C XP_005257731.1:p.=
XM_005257677.1:c.*277T>C XP_005257734.1:p.=
XM_006722085.1:c.*347T>C XP_006722148.1:p.=
XM_006722088.1:c.*347T>C XP_006722151.1:p.=
XM_006722089.1:c.*315T>C XP_006722152.1:p.=
XM_006722090.1:c.*315T>C XP_006722153.1:p.=
XM_011525255.1:c.*277T>C XP_011523557.1:p.=
XM_011525256.1:c.*277T>C XP_011523558.1:p.=
XM_011525257.1:c.*347T>C XP_011523559.1:p.=
NM_001135705.2:c.*347T>C VV NP_001129177.1:p.=
NM_001135706.2:c.*277T>C VV NP_001129178.1:p.=
NM_001135707.2:c.*1308T>C VV NP_001129179.1:p.=
NM_001321352.1:c.*277T>C VV NP_001308281.1:p.=
NM_001321353.1:c.*277T>C VV NP_001308282.1:p.=
NM_024722.3:c.*347T>C VV NP_078998.1:p.=
XM_006722085.2:c.*347T>C XP_006722148.1:p.=
XM_017025084.1:c.*277T>C XP_016880573.1:p.=
XM_017025085.1:c.*277T>C XP_016880574.1:p.=
XM_017025086.1:c.*277T>C XP_016880575.1:p.=
XM_017025087.1:c.*277T>C XP_016880576.1:p.=
XM_017025088.1:c.*277T>C XP_016880577.1:p.=
XM_017025089.2:c.*1138T>C XP_016880578.1:p.=
XM_017025090.1:c.*347T>C XP_016880579.1:p.=
XM_017025091.1:c.*347T>C XP_016880580.1:p.=
XM_017025092.2:c.*347T>C XP_016880581.1:p.=
XM_017025094.1:c.*1308T>C XP_016880583.1:p.=
XM_017025095.1:c.*347T>C XP_016880584.1:p.=
XM_017025096.1:c.*315T>C XP_016880585.1:p.=
XM_017025097.1:c.*347T>C XP_016880586.1:p.=
XM_017025098.1:c.*347T>C XP_016880587.1:p.=
XM_017025099.1:c.*315T>C XP_016880588.1:p.=
XM_024450949.1:c.*1138T>C XP_024306717.1:p.=
ENST00000321854.12:c.*347T>C ENSP00000314440.8:p.=
ENST00000398322.7:c.*347T>C ENSP00000381367.2:p.=
ENST00000431281.5:c.*277T>C ENSP00000405969.1:p.=
ENST00000585553.5:n.1983T>C
ENST00000591859.5:c.*277T>C ENSP00000465610.1:p.=
ENST00000592162.5:c.*315T>C ENSP00000466305.1:p.=