Canonical Allele Identifier: CA1556917434
Gene: PDE8B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.77222639_77222640delinsCT , CM000667.2:g.77222639_77222640delinsCT GRCh38
NC_000005.9:g.76518464_76518465delinsCT , CM000667.1:g.76518464_76518465delinsCT GRCh37
NC_000005.8:g.76554220_76554221delinsCT NCBI36
NG_023364.1:g.16759_16760delinsCT
NG_023364.2:g.47388_47389delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000264917.10:c.339+11375_339+11376delinsCT MANE Select ENSP00000264917.6:n.339+11375_339+11376de...
ENST00000646262.1:c.-33-89355_-33-89354delinsCT ENSP00000493971.1:n.-33-89355_-33-89354de...
ENST00000264917.9:c.339+11375_339+11376delinsCT ENSP00000264917.5:n.339+11375_339+11376de...
ENST00000333194.8:c.339+11375_339+11376delinsCT ENSP00000331336.4:n.339+11375_339+11376de...
ENST00000340978.7:c.339+11375_339+11376delinsCT ENSP00000345446.3:n.339+11375_339+11376de...
ENST00000342343.8:c.339+11375_339+11376delinsCT ENSP00000345646.4:n.339+11375_339+11376de...
ENST00000346042.7:c.339+11375_339+11376delinsCT ENSP00000330428.3:n.339+11375_339+11376de...
ENST00000502945.1:c.-153+8649_-153+8650delinsCT ENSP00000426200.1:n.-153+8649_-153+8650de...
ENST00000505926.5:c.-34+11375_-34+11376delinsCT ENSP00000425720.1:n.-34+11375_-34+11376de...
NM_001029851.2:c.339+11375_339+11376delinsCT NP_001025022.1:n.339+11375_339+11376delin...
NM_001029852.2:c.339+11375_339+11376delinsCT NP_001025023.1:n.339+11375_339+11376delin...
NM_001029853.2:c.339+11375_339+11376delinsCT NP_001025024.1:n.339+11375_339+11376delin...
NM_001029854.2:c.339+11375_339+11376delinsCT NP_001025025.1:n.339+11375_339+11376delin...
NM_003719.3:c.339+11375_339+11376delinsCT NP_003710.1:n.339+11375_339+11376delinsCT...
XM_005248621.3:c.339+11375_339+11376delinsCT XP_005248678.1:n.339+11375_339+11376delin...
XM_005248623.3:c.36+42153_36+42154delinsCT XP_005248680.1:n.36+42153_36+42154delinsC...
XM_005248624.3:c.36+42153_36+42154delinsCT XP_005248681.1:n.36+42153_36+42154delinsC...
XM_006714725.2:c.339+11375_339+11376delinsCT XP_006714788.1:n.339+11375_339+11376delin...
XM_006714726.2:c.339+11375_339+11376delinsCT XP_006714789.1:n.339+11375_339+11376delin...
XM_011543699.1:c.339+11375_339+11376delinsCT XP_011542001.1:n.339+11375_339+11376delin...
XM_011543700.1:c.339+11375_339+11376delinsCT XP_011542002.1:n.339+11375_339+11376delin...
XM_011543701.1:c.36+42153_36+42154delinsCT XP_011542003.1:n.36+42153_36+42154delinsC...
NM_001349748.1:c.339+11375_339+11376delinsCT NP_001336677.1:n.339+11375_339+11376delin...
NM_001349749.1:c.339+11375_339+11376delinsCT NP_001336678.1:n.339+11375_339+11376delin...
NM_001349750.1:c.36+42153_36+42154delinsCT NP_001336679.1:n.36+42153_36+42154delinsC...
NM_001349751.1:c.339+11375_339+11376delinsCT NP_001336680.1:n.339+11375_339+11376delin...
NM_001349752.1:c.36+42153_36+42154delinsCT NP_001336681.1:n.36+42153_36+42154delinsC...
NM_001349753.1:c.-31+11375_-31+11376delinsCT NP_001336682.1:n.-31+11375_-31+11376delin...
XM_005248623.4:c.36+42153_36+42154delinsCT XP_005248680.1:n.36+42153_36+42154delinsC...
XM_006714726.3:c.339+11375_339+11376delinsCT XP_006714789.1:n.339+11375_339+11376delin...
XM_011543699.3:c.339+11375_339+11376delinsCT XP_011542001.1:n.339+11375_339+11376delin...
XM_011543700.3:c.339+11375_339+11376delinsCT XP_011542002.1:n.339+11375_339+11376delin...
XM_017010005.2:c.339+11375_339+11376delinsCT XP_016865494.1:n.339+11375_339+11376delin...
XM_017010007.2:c.36+42153_36+42154delinsCT XP_016865496.1:n.36+42153_36+42154delinsC...
XM_017010008.2:c.36+42153_36+42154delinsCT XP_016865497.1:n.36+42153_36+42154delinsC...
XM_024446253.1:c.-34+12593_-34+12594delinsCT XP_024302021.1:n.-34+12593_-34+12594delin...
XM_024446254.1:c.-34+12593_-34+12594delinsCT XP_024302022.1:n.-34+12593_-34+12594delin...
NM_001029851.4:c.339+11375_339+11376delinsCT NP_001025022.1:n.339+11375_339+11376delin...
NM_001029852.4:c.339+11375_339+11376delinsCT NP_001025023.1:n.339+11375_339+11376delin...
NM_001029853.4:c.339+11375_339+11376delinsCT NP_001025024.1:n.339+11375_339+11376delin...
NM_001029854.4:c.339+11375_339+11376delinsCT NP_001025025.1:n.339+11375_339+11376delin...
NM_001349748.3:c.339+11375_339+11376delinsCT NP_001336677.1:n.339+11375_339+11376delin...
NM_001349749.3:c.339+11375_339+11376delinsCT NP_001336678.1:n.339+11375_339+11376delin...
NM_001349750.3:c.36+42153_36+42154delinsCT NP_001336679.1:n.36+42153_36+42154delinsC...
NM_001349751.3:c.339+11375_339+11376delinsCT NP_001336680.1:n.339+11375_339+11376delin...
NM_001349752.3:c.36+42153_36+42154delinsCT NP_001336681.1:n.36+42153_36+42154delinsC...
NM_001349753.2:c.-31+11375_-31+11376delinsCT NP_001336682.1:n.-31+11375_-31+11376delin...
NM_001376062.1:c.36+42153_36+42154delinsCT NP_001362991.1:n.36+42153_36+42154delinsC...
NM_001376063.1:c.339+11375_339+11376delinsCT NP_001362992.1:n.339+11375_339+11376delin...
NM_001376064.1:c.339+11375_339+11376delinsCT NP_001362993.1:n.339+11375_339+11376delin...
NM_001376065.1:c.339+11375_339+11376delinsCT NP_001362994.1:n.339+11375_339+11376delin...
NM_001376066.1:c.36+42153_36+42154delinsCT NP_001362995.1:n.36+42153_36+42154delinsC...
NM_001376067.1:c.-34+12593_-34+12594delinsCT NP_001362996.1:n.-34+12593_-34+12594delin...
NM_001376068.1:c.-31+12593_-31+12594delinsCT NP_001362997.1:n.-31+12593_-31+12594delin...
NM_001376069.1:c.36+42153_36+42154delinsCT NP_001362998.1:n.36+42153_36+42154delinsC...
NM_001376070.1:c.36+42153_36+42154delinsCT NP_001362999.1:n.36+42153_36+42154delinsC...
NM_001376071.1:c.36+42153_36+42154delinsCT NP_001363000.1:n.36+42153_36+42154delinsC...
NM_001376072.1:c.36+42153_36+42154delinsCT NP_001363001.1:n.36+42153_36+42154delinsC...
NM_001376073.1:c.36+42153_36+42154delinsCT NP_001363002.1:n.36+42153_36+42154delinsC...
NM_001376074.1:c.36+42153_36+42154delinsCT NP_001363003.1:n.36+42153_36+42154delinsC...
NM_001376075.1:c.-34+12593_-34+12594delinsCT NP_001363004.1:n.-34+12593_-34+12594delin...
NM_003719.5:c.339+11375_339+11376delinsCT MANE Select NP_003710.1:n.339+11375_339+11376delinsCT...