LDH info

Canonical Allele Identifier: CA387513577
Gene: SACS HGNC NCBI

Identifiers and link-outs to other resources

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
NM_001278055.1:c.9382C>A VV NP_001264984.1:p.Leu3128Ile
NM_014363.5:c.9823C>A VV NP_055178.3:p.Leu3275Ile
XM_005266338.1:c.9850C>A XP_005266395.1:p.Leu3284Ile
XM_011535038.1:c.9874C>A XP_011533340.1:p.Leu3292Ile
XM_011535039.1:c.9841C>A XP_011533341.1:p.Leu3281Ile
XM_005266338.2:c.9850C>A XP_005266395.1:p.Leu3284Ile
XM_011535039.2:c.9841C>A XP_011533341.1:p.Leu3281Ile
XM_017020539.1:c.9814C>A XP_016876028.1:p.Leu3272Ile
XM_024449337.1:c.9850C>A XP_024305105.1:p.Leu3284Ile
NM_014363.6:c.9823C>A VV MANE Preferred NP_055178.3:p.Leu3275Ile
NM_001278055.2:c.9382C>A VV NP_001264984.1:p.Leu3128Ile
ENST00000382292.7:c.9823C>A ENSP00000371729.3:p.Leu3275Ile
ENST00000382298.7:c.9823C>A ENSP00000371735.3:p.Leu3275Ile
ENST00000402364.1:c.7573C>A ENSP00000385844.1:p.Leu2525Ile
ENST00000423156.1:n.1058-4569C>A ENSP00000390925.1:p.=
ENST00000455470.5:n.2130-4569C>A