LDH info

Canonical Allele Identifier: CA6910558
Gene: SACS HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs772932340

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23334055G>C , CM000675.2:g.23334055G>C GRCh38
NC_000013.10:g.23908194G>C , CM000675.1:g.23908194G>C GRCh37
NC_000013.9:g.22806194G>C NCBI36
NG_012342.1:g.104648C>G

Transcript Alleles

HGVS Amino-acid change
NM_001278055.1:c.9380C>G VV NP_001264984.1:p.Thr3127Ser
NM_014363.5:c.9821C>G VV NP_055178.3:p.Thr3274Ser
XM_005266338.1:c.9848C>G XP_005266395.1:p.Thr3283Ser
XM_011535038.1:c.9872C>G XP_011533340.1:p.Thr3291Ser
XM_011535039.1:c.9839C>G XP_011533341.1:p.Thr3280Ser
XM_005266338.2:c.9848C>G XP_005266395.1:p.Thr3283Ser
XM_011535039.2:c.9839C>G XP_011533341.1:p.Thr3280Ser
XM_017020539.1:c.9812C>G XP_016876028.1:p.Thr3271Ser
XM_024449337.1:c.9848C>G XP_024305105.1:p.Thr3283Ser
NM_014363.6:c.9821C>G VV MANE Preferred NP_055178.3:p.Thr3274Ser
NM_001278055.2:c.9380C>G VV NP_001264984.1:p.Thr3127Ser
ENST00000382292.7:c.9821C>G ENSP00000371729.3:p.Thr3274Ser
ENST00000382298.7:c.9821C>G ENSP00000371735.3:p.Thr3274Ser
ENST00000402364.1:c.7571C>G ENSP00000385844.1:p.Thr2524Ser
ENST00000423156.1:n.1058-4571C>G ENSP00000390925.1:p.=
ENST00000455470.5:n.2130-4571C>G