LDH info

Canonical Allele Identifier: CA387513578
Gene: SACS HGNC NCBI

Identifiers and link-outs to other resources

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23334053G>C , CM000675.2:g.23334053G>C GRCh38
NC_000013.10:g.23908192G>C , CM000675.1:g.23908192G>C GRCh37
NC_000013.9:g.22806192G>C NCBI36
NG_012342.1:g.104650C>G

Transcript Alleles

HGVS Amino-acid change
NM_001278055.1:c.9382C>G VV NP_001264984.1:p.Leu3128Val
NM_014363.5:c.9823C>G VV NP_055178.3:p.Leu3275Val
XM_005266338.1:c.9850C>G XP_005266395.1:p.Leu3284Val
XM_011535038.1:c.9874C>G XP_011533340.1:p.Leu3292Val
XM_011535039.1:c.9841C>G XP_011533341.1:p.Leu3281Val
XM_005266338.2:c.9850C>G XP_005266395.1:p.Leu3284Val
XM_011535039.2:c.9841C>G XP_011533341.1:p.Leu3281Val
XM_017020539.1:c.9814C>G XP_016876028.1:p.Leu3272Val
XM_024449337.1:c.9850C>G XP_024305105.1:p.Leu3284Val
NM_014363.6:c.9823C>G VV MANE Preferred NP_055178.3:p.Leu3275Val
NM_001278055.2:c.9382C>G VV NP_001264984.1:p.Leu3128Val
ENST00000382292.7:c.9823C>G ENSP00000371729.3:p.Leu3275Val
ENST00000382298.7:c.9823C>G ENSP00000371735.3:p.Leu3275Val
ENST00000402364.1:c.7573C>G ENSP00000385844.1:p.Leu2525Val
ENST00000423156.1:n.1058-4569C>G ENSP00000390925.1:p.=
ENST00000455470.5:n.2130-4569C>G