LDH info

Canonical Allele Identifier: CA4262331
Gene: DDC HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs3735273

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.50529166C>T , CM000669.2:g.50529166C>T GRCh38
NC_000007.13:g.50596864C>T , CM000669.1:g.50596864C>T GRCh37
NC_000007.12:g.50564358C>T NCBI36
NG_008742.1:g.41291G>A

Transcript Alleles

HGVS Amino-acid change
NM_000790.3:c.570+42G>A VV NP_000781.1:p.=
NM_001082971.1:c.570+42G>A VV NP_001076440.1:p.=
NM_001242886.1:c.456+42G>A VV NP_001229815.1:p.=
NM_001242887.1:c.570+42G>A VV NP_001229816.1:p.=
NM_001242888.1:c.336+42G>A VV NP_001229817.1:p.=
NM_001242889.1:c.435+8694G>A VV NP_001229818.1:p.=
NM_001242890.1:c.570+42G>A VV NP_001229819.1:p.=
XM_005271745.3:c.456+42G>A XP_005271802.1:p.=
XM_011515161.1:c.219+42G>A XP_011513463.1:p.=
XM_005271745.4:c.456+42G>A XP_005271802.1:p.=
XM_011515161.2:c.513+42G>A XP_011513463.2:p.=
NM_001082971.2:c.570+42G>A VV MANE Preferred NP_001076440.2:p.=
NM_000790.4:c.570+42G>A VV NP_000781.2:p.=
NM_001242888.2:c.336+42G>A VV NP_001229817.2:p.=
NM_001242890.2:c.570+42G>A VV NP_001229819.2:p.=
ENST00000357936.9:c.570+42G>A ENSP00000350616.5:p.=
ENST00000380984.4:c.570+42G>A ENSP00000370371.4:p.=
ENST00000426377.5:c.336+42G>A ENSP00000395069.1:p.=
ENST00000430300.5:n.213-886G>A
ENST00000431062.5:c.435+8694G>A ENSP00000399184.1:p.=
ENST00000444124.6:c.570+42G>A ENSP00000403644.2:p.=
ENST00000444733.5:c.456+42G>A ENSP00000393724.1:p.=
ENST00000489162.1:n.369+42G>A
ENST00000613602.3:c.-11+13352G>A ENSP00000481751.1:p.=
ENST00000615193.4:c.435+8694G>A ENSP00000484104.1:p.=
ENST00000617822.4:c.570+42G>A ENSP00000478385.1:p.=
ENST00000622873.4:c.456+42G>A ENSP00000479110.1:p.=