LDH info

Canonical Allele Identifier: CA7019521
Gene: ABCC4 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs11568668

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.95186786C>T , CM000675.2:g.95186786C>T GRCh38
NC_000013.10:g.95839040C>T , CM000675.1:g.95839040C>T GRCh37
NC_000013.9:g.94637041C>T NCBI36
NG_050651.1:g.119661G>A

Transcript Alleles

HGVS Amino-acid change
NM_001105515.2:c.1460G>A VV NP_001098985.1:p.Gly487Glu
NM_001301829.1:c.1460G>A VV NP_001288758.1:p.Gly487Glu
NM_001301830.1:c.1235G>A VV NP_001288759.1:p.Gly412Glu
NM_005845.4:c.1460G>A VV NP_005836.2:p.Gly487Glu
XM_005254025.2:c.1331G>A XP_005254082.1:p.Gly444Glu
XM_006719914.1:c.1370G>A XP_006719977.1:p.Gly457Glu
XM_011521047.1:c.911G>A XP_011519349.1:p.Gly304Glu
XM_017020319.1:c.1331G>A XP_016875808.1:p.Gly444Glu
XM_017020320.2:c.1460G>A XP_016875809.1:p.Gly487Glu
XM_017020322.1:c.1331G>A XP_016875811.1:p.Gly444Glu
NM_001105515.3:c.1460G>A VV NP_001098985.1:p.Gly487Glu
NM_001301829.2:c.1460G>A VV NP_001288758.1:p.Gly487Glu
NM_001301830.2:c.1235G>A VV NP_001288759.1:p.Gly412Glu
NM_005845.5:c.1460G>A VV MANE Preferred NP_005836.2:p.Gly487Glu
ENST00000376887.8:c.1460G>A ENSP00000366084.4:p.Gly487Glu
ENST00000536256.3:c.1235G>A ENSP00000442024.1:p.Gly412Glu
ENST00000629385.1:c.1460G>A ENSP00000487081.1:p.Gly487Glu