LDH info

Canonical Allele Identifier: CA387513586
Gene: SACS HGNC NCBI

Identifiers and link-outs to other resources

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23334058T>A , CM000675.2:g.23334058T>A GRCh38
NC_000013.10:g.23908197T>A , CM000675.1:g.23908197T>A GRCh37
NC_000013.9:g.22806197T>A NCBI36
NG_012342.1:g.104645A>T

Transcript Alleles

HGVS Amino-acid change
NM_001278055.1:c.9377A>T VV NP_001264984.1:p.Asp3126Val
NM_014363.5:c.9818A>T VV NP_055178.3:p.Asp3273Val
XM_005266338.1:c.9845A>T XP_005266395.1:p.Asp3282Val
XM_011535038.1:c.9869A>T XP_011533340.1:p.Asp3290Val
XM_011535039.1:c.9836A>T XP_011533341.1:p.Asp3279Val
XM_005266338.2:c.9845A>T XP_005266395.1:p.Asp3282Val
XM_011535039.2:c.9836A>T XP_011533341.1:p.Asp3279Val
XM_017020539.1:c.9809A>T XP_016876028.1:p.Asp3270Val
XM_024449337.1:c.9845A>T XP_024305105.1:p.Asp3282Val
NM_014363.6:c.9818A>T VV MANE Preferred NP_055178.3:p.Asp3273Val
NM_001278055.2:c.9377A>T VV NP_001264984.1:p.Asp3126Val
ENST00000382292.7:c.9818A>T ENSP00000371729.3:p.Asp3273Val
ENST00000382298.7:c.9818A>T ENSP00000371735.3:p.Asp3273Val
ENST00000402364.1:c.7568A>T ENSP00000385844.1:p.Asp2523Val
ENST00000423156.1:n.1058-4574A>T ENSP00000390925.1:p.=
ENST00000455470.5:n.2130-4574A>T