LDH info

Canonical Allele Identifier: CA12466938
Gene: DDC HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs11761683

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.50475181C>T , CM000669.2:g.50475181C>T GRCh38
NC_000007.13:g.50542879C>T , CM000669.1:g.50542879C>T GRCh37
NC_000007.12:g.50510373C>T NCBI36
NG_008742.1:g.95276G>A

Transcript Alleles

HGVS Amino-acid change
NM_000790.3:c.1041+1443G>A VV NP_000781.1:p.=
NM_001082971.1:c.1041+1443G>A VV NP_001076440.1:p.=
NM_001242886.1:c.927+1443G>A VV NP_001229815.1:p.=
NM_001242887.1:c.897+1443G>A VV NP_001229816.1:p.=
NM_001242888.1:c.807+1443G>A VV NP_001229817.1:p.=
NM_001242889.1:c.762+1443G>A VV NP_001229818.1:p.=
XM_005271745.3:c.927+1443G>A XP_005271802.1:p.=
XM_011515161.1:c.690+1443G>A XP_011513463.1:p.=
XM_005271745.4:c.927+1443G>A XP_005271802.1:p.=
XM_011515161.2:c.984+1443G>A XP_011513463.2:p.=
NM_001082971.2:c.1041+1443G>A VV MANE Preferred NP_001076440.2:p.=
NM_000790.4:c.1041+1443G>A VV NP_000781.2:p.=
NM_001242888.2:c.807+1443G>A VV NP_001229817.2:p.=
ENST00000357936.9:c.1041+1443G>A ENSP00000350616.5:p.=
ENST00000426377.5:c.807+1443G>A ENSP00000395069.1:p.=
ENST00000430300.5:n.683+1443G>A
ENST00000431062.5:c.762+1443G>A ENSP00000399184.1:p.=
ENST00000444124.6:c.1041+1443G>A ENSP00000403644.2:p.=
ENST00000444733.5:c.*142+1443G>A ENSP00000393724.1:p.=
ENST00000494914.1:n.197+1443G>A
ENST00000613602.3:c.-10-27884G>A ENSP00000481751.1:p.=
ENST00000615193.4:c.762+1443G>A ENSP00000484104.1:p.=
ENST00000617822.4:c.897+1443G>A ENSP00000478385.1:p.=
ENST00000622873.4:c.927+1443G>A ENSP00000479110.1:p.=