LDH info

Canonical Allele Identifier: CA6910541
Gene: SACS HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs761124250

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23333961G>A , CM000675.2:g.23333961G>A GRCh38
NC_000013.10:g.23908100G>A , CM000675.1:g.23908100G>A GRCh37
NC_000013.9:g.22806100G>A NCBI36
NG_012342.1:g.104742C>T

Transcript Alleles

HGVS Amino-acid change
NM_001278055.1:c.9474C>T VV NP_001264984.1:p.Ser3158=
NM_014363.5:c.9915C>T VV NP_055178.3:p.Ser3305=
XM_005266338.1:c.9942C>T XP_005266395.1:p.Ser3314=
XM_011535038.1:c.9966C>T XP_011533340.1:p.Ser3322=
XM_011535039.1:c.9933C>T XP_011533341.1:p.Ser3311=
XM_005266338.2:c.9942C>T XP_005266395.1:p.Ser3314=
XM_011535039.2:c.9933C>T XP_011533341.1:p.Ser3311=
XM_017020539.1:c.9906C>T XP_016876028.1:p.Ser3302=
XM_024449337.1:c.9942C>T XP_024305105.1:p.Ser3314=
NM_014363.6:c.9915C>T VV MANE Preferred NP_055178.3:p.Ser3305=
NM_001278055.2:c.9474C>T VV NP_001264984.1:p.Ser3158=
ENST00000382292.7:c.9915C>T ENSP00000371729.3:p.Ser3305=
ENST00000382298.7:c.9915C>T ENSP00000371735.3:p.Ser3305=
ENST00000402364.1:c.7665C>T ENSP00000385844.1:p.Ser2555=
ENST00000423156.1:n.1058-4477C>T ENSP00000390925.1:p.=
ENST00000455470.5:n.2130-4477C>T