LDH info

Canonical Allele Identifier: CA387513583
Gene: SACS HGNC NCBI

Identifiers and link-outs to other resources

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23334056T>G , CM000675.2:g.23334056T>G GRCh38
NC_000013.10:g.23908195T>G , CM000675.1:g.23908195T>G GRCh37
NC_000013.9:g.22806195T>G NCBI36
NG_012342.1:g.104647A>C

Transcript Alleles

HGVS Amino-acid change
NM_001278055.1:c.9379A>C VV NP_001264984.1:p.Thr3127Pro
NM_014363.5:c.9820A>C VV NP_055178.3:p.Thr3274Pro
XM_005266338.1:c.9847A>C XP_005266395.1:p.Thr3283Pro
XM_011535038.1:c.9871A>C XP_011533340.1:p.Thr3291Pro
XM_011535039.1:c.9838A>C XP_011533341.1:p.Thr3280Pro
XM_005266338.2:c.9847A>C XP_005266395.1:p.Thr3283Pro
XM_011535039.2:c.9838A>C XP_011533341.1:p.Thr3280Pro
XM_017020539.1:c.9811A>C XP_016876028.1:p.Thr3271Pro
XM_024449337.1:c.9847A>C XP_024305105.1:p.Thr3283Pro
NM_014363.6:c.9820A>C VV MANE Preferred NP_055178.3:p.Thr3274Pro
NM_001278055.2:c.9379A>C VV NP_001264984.1:p.Thr3127Pro
ENST00000382292.7:c.9820A>C ENSP00000371729.3:p.Thr3274Pro
ENST00000382298.7:c.9820A>C ENSP00000371735.3:p.Thr3274Pro
ENST00000402364.1:c.7570A>C ENSP00000385844.1:p.Thr2524Pro
ENST00000423156.1:n.1058-4572A>C ENSP00000390925.1:p.=
ENST00000455470.5:n.2130-4572A>C