Canonical Allele Identifier: CA1556932742

Gene: PDE8B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.77301555C= , CM000667.2:g.77301555C=	GRCh38
NC_000005.9:g.76597380C= , CM000667.1:g.76597380C=	GRCh37
NC_000005.8:g.76633136C=	NCBI36
NG_023364.1:g.95675C=
NG_023364.2:g.126304C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264917.10:c.340-10439C= MANE Select	ENSP00000264917.6:n.340-10439C=
ENST00000646262.1:c.-33-10439C=	ENSP00000493971.1:n.-33-10439C=
ENST00000264917.9:c.340-10439C=	ENSP00000264917.5:n.340-10439C=
ENST00000333194.8:c.340-10439C=	ENSP00000331336.4:n.340-10439C=
ENST00000340978.7:c.340-10439C=	ENSP00000345446.3:n.340-10439C=
ENST00000342343.8:c.340-23984C=	ENSP00000345646.4:n.340-23984C=
ENST00000346042.7:c.340-10439C=	ENSP00000330428.3:n.340-10439C=
ENST00000502945.1:c.-33-10439C=	ENSP00000426200.1:n.-33-10439C=
ENST00000505926.5:c.-33-10439C=	ENSP00000425720.1:n.-33-10439C=
NM_001029851.2:c.340-10439C=	NP_001025022.1:n.340-10439C=
NM_001029852.2:c.340-10439C=	NP_001025023.1:n.340-10439C=
NM_001029853.2:c.340-23984C=	NP_001025024.1:n.340-23984C=
NM_001029854.2:c.340-10439C=	NP_001025025.1:n.340-10439C=
NM_003719.3:c.340-10439C=	NP_003710.1:n.340-10439C=
XM_005248621.3:c.340-10442C=	XP_005248678.1:n.340-10442C=
XM_005248623.3:c.37-10439C=	XP_005248680.1:n.37-10439C=
XM_005248624.3:c.37-10442C=	XP_005248681.1:n.37-10442C=
XM_006714725.2:c.402+2693C=	XP_006714788.1:n.402+2693C=
XM_006714726.2:c.402+2693C=	XP_006714789.1:n.402+2693C=
XM_011543699.1:c.402+2693C=	XP_011542001.1:n.402+2693C=
XM_011543700.1:c.402+2693C=	XP_011542002.1:n.402+2693C=
XM_011543701.1:c.99+2693C=	XP_011542003.1:n.99+2693C=
NM_001349748.1:c.340-10442C=	NP_001336677.1:n.340-10442C=
NM_001349749.1:c.402+2693C=	NP_001336678.1:n.402+2693C=
NM_001349750.1:c.99+2693C=	NP_001336679.1:n.99+2693C=
NM_001349751.1:c.340-10442C=	NP_001336680.1:n.340-10442C=
NM_001349752.1:c.37-10442C=	NP_001336681.1:n.37-10442C=
NM_001349753.1:c.-30-10442C=	NP_001336682.1:n.-30-10442C=
XM_005248623.4:c.37-10439C=	XP_005248680.1:n.37-10439C=
XM_006714726.3:c.402+2693C=	XP_006714789.1:n.402+2693C=
XM_011543699.3:c.402+2693C=	XP_011542001.1:n.402+2693C=
XM_011543700.3:c.402+2693C=	XP_011542002.1:n.402+2693C=
XM_017010005.2:c.340-10442C=	XP_016865494.1:n.340-10442C=
XM_017010007.2:c.37-10439C=	XP_016865496.1:n.37-10439C=
XM_017010008.2:c.37-10439C=	XP_016865497.1:n.37-10439C=
XM_024446253.1:c.-33-10439C=	XP_024302021.1:n.-33-10439C=
XM_024446254.1:c.-33-10439C=	XP_024302022.1:n.-33-10439C=
NM_001029851.4:c.340-10439C=	NP_001025022.1:n.340-10439C=
NM_001029852.4:c.340-10439C=	NP_001025023.1:n.340-10439C=
NM_001029853.4:c.340-23984C=	NP_001025024.1:n.340-23984C=
NM_001029854.4:c.340-10439C=	NP_001025025.1:n.340-10439C=
NM_001349748.3:c.340-10442C=	NP_001336677.1:n.340-10442C=
NM_001349749.3:c.402+2693C=	NP_001336678.1:n.402+2693C=
NM_001349750.3:c.99+2693C=	NP_001336679.1:n.99+2693C=
NM_001349751.3:c.340-10442C=	NP_001336680.1:n.340-10442C=
NM_001349752.3:c.37-10442C=	NP_001336681.1:n.37-10442C=
NM_001349753.2:c.-30-10442C=	NP_001336682.1:n.-30-10442C=
NM_001376062.1:c.37-10439C=	NP_001362991.1:n.37-10439C=
NM_001376063.1:c.340-10439C=	NP_001362992.1:n.340-10439C=
NM_001376064.1:c.340-10439C=	NP_001362993.1:n.340-10439C=
NM_001376065.1:c.340-10442C=	NP_001362994.1:n.340-10442C=
NM_001376066.1:c.37-23984C=	NP_001362995.1:n.37-23984C=
NM_001376067.1:c.-33-10439C=	NP_001362996.1:n.-33-10439C=
NM_001376068.1:c.-30-10442C=	NP_001362997.1:n.-30-10442C=
NM_001376069.1:c.99+2693C=	NP_001362998.1:n.99+2693C=
NM_001376070.1:c.37-10439C=	NP_001362999.1:n.37-10439C=
NM_001376071.1:c.37-10442C=	NP_001363000.1:n.37-10442C=
NM_001376072.1:c.37-10439C=	NP_001363001.1:n.37-10439C=
NM_001376073.1:c.37-10439C=	NP_001363002.1:n.37-10439C=
NM_001376074.1:c.37-23984C=	NP_001363003.1:n.37-23984C=
NM_001376075.1:c.-33-10439C=	NP_001363004.1:n.-33-10439C=
NM_003719.5:c.340-10439C= MANE Select	NP_003710.1:n.340-10439C=