LDH info

Canonical Allele Identifier: CA387513386
Gene: SACS HGNC NCBI

Identifiers and link-outs to other resources

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23333963T>G , CM000675.2:g.23333963T>G GRCh38
NC_000013.10:g.23908102T>G , CM000675.1:g.23908102T>G GRCh37
NC_000013.9:g.22806102T>G NCBI36
NG_012342.1:g.104740A>C

Transcript Alleles

HGVS Amino-acid change
NM_001278055.1:c.9472A>C VV NP_001264984.1:p.Ser3158Arg
NM_014363.5:c.9913A>C VV NP_055178.3:p.Ser3305Arg
XM_005266338.1:c.9940A>C XP_005266395.1:p.Ser3314Arg
XM_011535038.1:c.9964A>C XP_011533340.1:p.Ser3322Arg
XM_011535039.1:c.9931A>C XP_011533341.1:p.Ser3311Arg
XM_005266338.2:c.9940A>C XP_005266395.1:p.Ser3314Arg
XM_011535039.2:c.9931A>C XP_011533341.1:p.Ser3311Arg
XM_017020539.1:c.9904A>C XP_016876028.1:p.Ser3302Arg
XM_024449337.1:c.9940A>C XP_024305105.1:p.Ser3314Arg
NM_014363.6:c.9913A>C VV MANE Preferred NP_055178.3:p.Ser3305Arg
NM_001278055.2:c.9472A>C VV NP_001264984.1:p.Ser3158Arg
ENST00000382292.7:c.9913A>C ENSP00000371729.3:p.Ser3305Arg
ENST00000382298.7:c.9913A>C ENSP00000371735.3:p.Ser3305Arg
ENST00000402364.1:c.7663A>C ENSP00000385844.1:p.Ser2555Arg
ENST00000423156.1:n.1058-4479A>C ENSP00000390925.1:p.=
ENST00000455470.5:n.2130-4479A>C