LDH info

Canonical Allele Identifier: CA483159503
Gene: SACS HGNC NCBI

Identifiers and link-outs to other resources

MyVariant Identifiers: chr13:g.23908193A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23334054A>T , CM000675.2:g.23334054A>T GRCh38
NC_000013.10:g.23908193A>T , CM000675.1:g.23908193A>T GRCh37
NC_000013.9:g.22806193A>T NCBI36
NG_012342.1:g.104649T>A

Transcript Alleles

HGVS Amino-acid change
NM_001278055.1:c.9381T>A VV NP_001264984.1:p.Thr3127=
NM_014363.5:c.9822T>A VV NP_055178.3:p.Thr3274=
XM_005266338.1:c.9849T>A XP_005266395.1:p.Thr3283=
XM_011535038.1:c.9873T>A XP_011533340.1:p.Thr3291=
XM_011535039.1:c.9840T>A XP_011533341.1:p.Thr3280=
XM_005266338.2:c.9849T>A XP_005266395.1:p.Thr3283=
XM_011535039.2:c.9840T>A XP_011533341.1:p.Thr3280=
XM_017020539.1:c.9813T>A XP_016876028.1:p.Thr3271=
XM_024449337.1:c.9849T>A XP_024305105.1:p.Thr3283=
NM_014363.6:c.9822T>A VV MANE Preferred NP_055178.3:p.Thr3274=
NM_001278055.2:c.9381T>A VV NP_001264984.1:p.Thr3127=
ENST00000382292.7:c.9822T>A ENSP00000371729.3:p.Thr3274=
ENST00000382298.7:c.9822T>A ENSP00000371735.3:p.Thr3274=
ENST00000402364.1:c.7572T>A ENSP00000385844.1:p.Thr2524=
ENST00000423156.1:n.1058-4570T>A ENSP00000390925.1:p.=
ENST00000455470.5:n.2130-4570T>A