LDH info

Canonical Allele Identifier: CA387513563
Gene: SACS HGNC NCBI

Identifiers and link-outs to other resources

COSMIC: COSM277152

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23334047C>A , CM000675.2:g.23334047C>A GRCh38
NC_000013.10:g.23908186C>A , CM000675.1:g.23908186C>A GRCh37
NC_000013.9:g.22806186C>A NCBI36
NG_012342.1:g.104656G>T

Transcript Alleles

HGVS Amino-acid change
NM_001278055.1:c.9388G>T VV NP_001264984.1:p.Asp3130Tyr
NM_014363.5:c.9829G>T VV NP_055178.3:p.Asp3277Tyr
XM_005266338.1:c.9856G>T XP_005266395.1:p.Asp3286Tyr
XM_011535038.1:c.9880G>T XP_011533340.1:p.Asp3294Tyr
XM_011535039.1:c.9847G>T XP_011533341.1:p.Asp3283Tyr
XM_005266338.2:c.9856G>T XP_005266395.1:p.Asp3286Tyr
XM_011535039.2:c.9847G>T XP_011533341.1:p.Asp3283Tyr
XM_017020539.1:c.9820G>T XP_016876028.1:p.Asp3274Tyr
XM_024449337.1:c.9856G>T XP_024305105.1:p.Asp3286Tyr
NM_014363.6:c.9829G>T VV MANE Preferred NP_055178.3:p.Asp3277Tyr
NM_001278055.2:c.9388G>T VV NP_001264984.1:p.Asp3130Tyr
ENST00000382292.7:c.9829G>T ENSP00000371729.3:p.Asp3277Tyr
ENST00000382298.7:c.9829G>T ENSP00000371735.3:p.Asp3277Tyr
ENST00000402364.1:c.7579G>T ENSP00000385844.1:p.Asp2527Tyr
ENST00000423156.1:n.1058-4563G>T ENSP00000390925.1:p.=
ENST00000455470.5:n.2130-4563G>T