LDH info

Canonical Allele Identifier: CA12001455
Gene: PDE4D HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10052657

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.59111944C>A , CM000667.2:g.59111944C>A GRCh38
NC_000005.9:g.58407771C>A , CM000667.1:g.58407771C>A GRCh37
NC_000005.8:g.58443528C>A NCBI36
NG_027957.1:g.1381155G>T
NG_027957.2:g.1417386G>T

Transcript Alleles

HGVS Amino-acid change
NM_001104631.1:c.808+68651G>T VV NP_001098101.1:p.=
NM_001165899.1:c.625+68651G>T VV NP_001159371.1:p.=
NM_001197218.1:c.616+68651G>T VV NP_001184147.1:p.=
NM_001197219.1:c.442+68651G>T VV NP_001184148.1:p.=
NM_001197220.1:c.418+68651G>T VV NP_001184149.1:p.=
NM_006203.4:c.400+68651G>T VV NP_006194.2:p.=
XM_005248537.2:c.478+68651G>T XP_005248594.1:p.=
XM_005248538.3:c.400+68651G>T XP_005248595.1:p.=
XM_011543469.1:c.772+68651G>T XP_011541771.1:p.=
XM_011543470.1:c.772+68651G>T XP_011541772.1:p.=
XM_011543471.1:c.625+68651G>T XP_011541773.1:p.=
XM_011543472.1:c.625+68651G>T XP_011541774.1:p.=
XM_011543473.1:c.625+68651G>T XP_011541775.1:p.=
XM_011543474.1:c.595+68651G>T XP_011541776.1:p.=
XM_011543475.1:c.442+68651G>T XP_011541777.1:p.=
XM_011543476.1:c.388+68651G>T XP_011541778.1:p.=
XM_011543477.1:c.367+68651G>T XP_011541779.1:p.=
XM_011543478.1:c.304+68651G>T XP_011541780.1:p.=
XM_011543479.1:c.304+68651G>T XP_011541781.1:p.=
NM_001349241.1:c.595+68651G>T VV NP_001336170.1:p.=
NM_001349242.1:c.478+68651G>T VV NP_001336171.1:p.=
NM_001349243.1:c.40+68651G>T VV NP_001336172.1:p.=
NM_001364599.1:c.625+68651G>T VV NP_001351528.1:p.=
NM_001364603.1:c.-142-20819G>T VV NP_001351532.1:p.=
NM_001364604.1:c.40+68651G>T VV NP_001351533.1:p.=
XM_011543470.2:c.772+68651G>T XP_011541772.1:p.=
XM_011543471.2:c.625+68651G>T XP_011541773.1:p.=
XM_017009565.1:c.772+68651G>T XP_016865054.1:p.=
XM_017009566.1:c.625+68651G>T XP_016865055.1:p.=
XM_017009567.1:c.610+68651G>T XP_016865056.1:p.=
XM_024446110.1:c.772+68651G>T XP_024301878.1:p.=
XM_024446112.1:c.625+68651G>T XP_024301880.1:p.=
NM_001104631.2:c.808+68651G>T VV MANE Preferred NP_001098101.1:p.=
ENST00000309641.10:n.617-20819G>T ENSP00000308485.6:p.=
ENST00000340635.10:c.808+68651G>T ENSP00000345502.6:p.=
ENST00000360047.9:c.400+68651G>T ENSP00000353152.5:p.=
ENST00000405053.7:n.471+68651G>T
ENST00000405755.6:c.442+68651G>T ENSP00000384806.2:p.=
ENST00000502484.6:c.625+68651G>T ENSP00000423094.2:p.=
ENST00000503258.5:c.418+68651G>T ENSP00000425605.1:p.=
ENST00000505453.1:c.-98-72973G>T ENSP00000421013.1:p.=
ENST00000507116.5:c.616+68651G>T ENSP00000424852.1:p.=
ENST00000546160.5:c.415+68651G>T ENSP00000442734.2:p.=