LDH info

Canonical Allele Identifier: CA387513378
Gene: SACS HGNC NCBI

Identifiers and link-outs to other resources

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23333960G>T , CM000675.2:g.23333960G>T GRCh38
NC_000013.10:g.23908099G>T , CM000675.1:g.23908099G>T GRCh37
NC_000013.9:g.22806099G>T NCBI36
NG_012342.1:g.104743C>A

Transcript Alleles

HGVS Amino-acid change
NM_001278055.1:c.9475C>A VV NP_001264984.1:p.Leu3159Ile
NM_014363.5:c.9916C>A VV NP_055178.3:p.Leu3306Ile
XM_005266338.1:c.9943C>A XP_005266395.1:p.Leu3315Ile
XM_011535038.1:c.9967C>A XP_011533340.1:p.Leu3323Ile
XM_011535039.1:c.9934C>A XP_011533341.1:p.Leu3312Ile
XM_005266338.2:c.9943C>A XP_005266395.1:p.Leu3315Ile
XM_011535039.2:c.9934C>A XP_011533341.1:p.Leu3312Ile
XM_017020539.1:c.9907C>A XP_016876028.1:p.Leu3303Ile
XM_024449337.1:c.9943C>A XP_024305105.1:p.Leu3315Ile
NM_014363.6:c.9916C>A VV MANE Preferred NP_055178.3:p.Leu3306Ile
NM_001278055.2:c.9475C>A VV NP_001264984.1:p.Leu3159Ile
ENST00000382292.7:c.9916C>A ENSP00000371729.3:p.Leu3306Ile
ENST00000382298.7:c.9916C>A ENSP00000371735.3:p.Leu3306Ile
ENST00000402364.1:c.7666C>A ENSP00000385844.1:p.Leu2556Ile
ENST00000423156.1:n.1058-4476C>A ENSP00000390925.1:p.=
ENST00000455470.5:n.2130-4476C>A