LDH info

Canonical Allele Identifier: CA387513365
Gene: SACS HGNC NCBI

Identifiers and link-outs to other resources

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23333954G>C , CM000675.2:g.23333954G>C GRCh38
NC_000013.10:g.23908093G>C , CM000675.1:g.23908093G>C GRCh37
NC_000013.9:g.22806093G>C NCBI36
NG_012342.1:g.104749C>G

Transcript Alleles

HGVS Amino-acid change
NM_001278055.1:c.9481C>G VV NP_001264984.1:p.His3161Asp
NM_014363.5:c.9922C>G VV NP_055178.3:p.His3308Asp
XM_005266338.1:c.9949C>G XP_005266395.1:p.His3317Asp
XM_011535038.1:c.9973C>G XP_011533340.1:p.His3325Asp
XM_011535039.1:c.9940C>G XP_011533341.1:p.His3314Asp
XM_005266338.2:c.9949C>G XP_005266395.1:p.His3317Asp
XM_011535039.2:c.9940C>G XP_011533341.1:p.His3314Asp
XM_017020539.1:c.9913C>G XP_016876028.1:p.His3305Asp
XM_024449337.1:c.9949C>G XP_024305105.1:p.His3317Asp
NM_014363.6:c.9922C>G VV MANE Preferred NP_055178.3:p.His3308Asp
NM_001278055.2:c.9481C>G VV NP_001264984.1:p.His3161Asp
ENST00000382292.7:c.9922C>G ENSP00000371729.3:p.His3308Asp
ENST00000382298.7:c.9922C>G ENSP00000371735.3:p.His3308Asp
ENST00000402364.1:c.7672C>G ENSP00000385844.1:p.His2558Asp
ENST00000423156.1:n.1058-4470C>G ENSP00000390925.1:p.=
ENST00000455470.5:n.2130-4470C>G