LDH info

Canonical Allele Identifier: CA387513383
Gene: SACS HGNC NCBI

Identifiers and link-outs to other resources

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23333962C>G , CM000675.2:g.23333962C>G GRCh38
NC_000013.10:g.23908101C>G , CM000675.1:g.23908101C>G GRCh37
NC_000013.9:g.22806101C>G NCBI36
NG_012342.1:g.104741G>C

Transcript Alleles

HGVS Amino-acid change
NM_001278055.1:c.9473G>C VV NP_001264984.1:p.Ser3158Thr
NM_014363.5:c.9914G>C VV NP_055178.3:p.Ser3305Thr
XM_005266338.1:c.9941G>C XP_005266395.1:p.Ser3314Thr
XM_011535038.1:c.9965G>C XP_011533340.1:p.Ser3322Thr
XM_011535039.1:c.9932G>C XP_011533341.1:p.Ser3311Thr
XM_005266338.2:c.9941G>C XP_005266395.1:p.Ser3314Thr
XM_011535039.2:c.9932G>C XP_011533341.1:p.Ser3311Thr
XM_017020539.1:c.9905G>C XP_016876028.1:p.Ser3302Thr
XM_024449337.1:c.9941G>C XP_024305105.1:p.Ser3314Thr
NM_014363.6:c.9914G>C VV MANE Preferred NP_055178.3:p.Ser3305Thr
NM_001278055.2:c.9473G>C VV NP_001264984.1:p.Ser3158Thr
ENST00000382292.7:c.9914G>C ENSP00000371729.3:p.Ser3305Thr
ENST00000382298.7:c.9914G>C ENSP00000371735.3:p.Ser3305Thr
ENST00000402364.1:c.7664G>C ENSP00000385844.1:p.Ser2555Thr
ENST00000423156.1:n.1058-4478G>C ENSP00000390925.1:p.=
ENST00000455470.5:n.2130-4478G>C