Canonical Allele Identifier: CA2674332518

Gene: PDE8B

Linked Data

• gnomAD v4: 5-77331502-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.77331502T>C , CM000667.2:g.77331502T>C	GRCh38
NC_000005.9:g.76627327T>C , CM000667.1:g.76627327T>C	GRCh37
NC_000005.8:g.76663083T>C	NCBI36
NG_023364.1:g.125622T>C
NG_023364.2:g.156251T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264917.10:c.708+43T>C MANE Select	ENSP00000264917.6:n.708+43T>C
ENST00000646262.1:c.336+43T>C	ENSP00000493971.1:n.336+43T>C
ENST00000264917.9:c.708+43T>C	ENSP00000264917.5:n.708+43T>C
ENST00000333194.8:c.708+43T>C	ENSP00000331336.4:n.708+43T>C
ENST00000340978.7:c.708+43T>C	ENSP00000345446.3:n.708+43T>C
ENST00000342343.8:c.648+43T>C	ENSP00000345646.4:n.648+43T>C
ENST00000346042.7:c.708+43T>C	ENSP00000330428.3:n.708+43T>C
ENST00000503963.1:c.-7+43T>C	ENSP00000422861.1:n.-7+43T>C
NM_001029851.2:c.708+43T>C	NP_001025022.1:n.708+43T>C
NM_001029852.2:c.708+43T>C	NP_001025023.1:n.708+43T>C
NM_001029853.2:c.648+43T>C	NP_001025024.1:n.648+43T>C
NM_001029854.2:c.708+43T>C	NP_001025025.1:n.708+43T>C
NM_003719.3:c.708+43T>C	NP_003710.1:n.708+43T>C
XM_005248621.3:c.705+43T>C	XP_005248678.1:n.705+43T>C
XM_005248623.3:c.405+43T>C	XP_005248680.1:n.405+43T>C
XM_005248624.3:c.402+43T>C	XP_005248681.1:n.402+43T>C
XM_006714725.2:c.771+43T>C	XP_006714788.1:n.771+43T>C
XM_006714726.2:c.768+43T>C	XP_006714789.1:n.768+43T>C
XM_011543699.1:c.771+43T>C	XP_011542001.1:n.771+43T>C
XM_011543700.1:c.771+43T>C	XP_011542002.1:n.771+43T>C
XM_011543701.1:c.468+43T>C	XP_011542003.1:n.468+43T>C
XM_011543702.1:c.375+43T>C	XP_011542004.1:n.375+43T>C
XM_011543703.1:c.393+43T>C	XP_011542005.1:n.393+43T>C
XM_011543704.1:c.-7+43T>C	XP_011542006.1:n.-7+43T>C
NM_001349748.1:c.705+43T>C	NP_001336677.1:n.705+43T>C
NM_001349749.1:c.771+43T>C	NP_001336678.1:n.771+43T>C
NM_001349750.1:c.468+43T>C	NP_001336679.1:n.468+43T>C
NM_001349751.1:c.705+43T>C	NP_001336680.1:n.705+43T>C
NM_001349752.1:c.402+43T>C	NP_001336681.1:n.402+43T>C
NM_001349753.1:c.336+43T>C	NP_001336682.1:n.336+43T>C
XM_005248623.4:c.405+43T>C	XP_005248680.1:n.405+43T>C
XM_006714726.3:c.768+43T>C	XP_006714789.1:n.768+43T>C
XM_011543699.3:c.771+43T>C	XP_011542001.1:n.771+43T>C
XM_011543700.3:c.771+43T>C	XP_011542002.1:n.771+43T>C
XM_011543704.2:c.-7+43T>C	XP_011542006.1:n.-7+43T>C
XM_017010005.2:c.705+43T>C	XP_016865494.1:n.705+43T>C
XM_017010007.2:c.405+43T>C	XP_016865496.1:n.405+43T>C
XM_017010008.2:c.405+43T>C	XP_016865497.1:n.405+43T>C
XM_024446253.1:c.336+43T>C	XP_024302021.1:n.336+43T>C
XM_024446254.1:c.336+43T>C	XP_024302022.1:n.336+43T>C
NM_001029851.4:c.708+43T>C	NP_001025022.1:n.708+43T>C
NM_001029852.4:c.708+43T>C	NP_001025023.1:n.708+43T>C
NM_001029853.4:c.648+43T>C	NP_001025024.1:n.648+43T>C
NM_001029854.4:c.708+43T>C	NP_001025025.1:n.708+43T>C
NM_001349748.3:c.705+43T>C	NP_001336677.1:n.705+43T>C
NM_001349749.3:c.771+43T>C	NP_001336678.1:n.771+43T>C
NM_001349750.3:c.468+43T>C	NP_001336679.1:n.468+43T>C
NM_001349751.3:c.705+43T>C	NP_001336680.1:n.705+43T>C
NM_001349752.3:c.402+43T>C	NP_001336681.1:n.402+43T>C
NM_001349753.2:c.336+43T>C	NP_001336682.1:n.336+43T>C
NM_001376062.1:c.405+43T>C	NP_001362991.1:n.405+43T>C
NM_001376063.1:c.708+43T>C	NP_001362992.1:n.708+43T>C
NM_001376064.1:c.708+43T>C	NP_001362993.1:n.708+43T>C
NM_001376065.1:c.705+43T>C	NP_001362994.1:n.705+43T>C
NM_001376066.1:c.345+43T>C	NP_001362995.1:n.345+43T>C
NM_001376067.1:c.336+43T>C	NP_001362996.1:n.336+43T>C
NM_001376068.1:c.336+43T>C	NP_001362997.1:n.336+43T>C
NM_001376069.1:c.465+43T>C	NP_001362998.1:n.465+43T>C
NM_001376070.1:c.405+43T>C	NP_001362999.1:n.405+43T>C
NM_001376071.1:c.402+43T>C	NP_001363000.1:n.402+43T>C
NM_001376072.1:c.405+43T>C	NP_001363001.1:n.405+43T>C
NM_001376073.1:c.405+43T>C	NP_001363002.1:n.405+43T>C
NM_001376074.1:c.345+43T>C	NP_001363003.1:n.345+43T>C
NM_001376075.1:c.336+43T>C	NP_001363004.1:n.336+43T>C
NM_003719.5:c.708+43T>C MANE Select	NP_003710.1:n.708+43T>C