Canonical Allele Identifier: CA10620598

Gene: PDE4D

Linked Data

• ClinVar Variation Id: 353910
• ClinVar RCV Id: RCV000262051
• dbSNP Id: rs11950492
• gnomAD v2: 5-58265231-A-G
• gnomAD v3: 5-58969404-A-G
• gnomAD v4: 5-58969404-A-G
• MyVariant Identifiers: chr5:g.58265231A>G (hg19) ; chr5:g.58969404A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.58969404A>G , CM000667.2:g.58969404A>G	GRCh38
NC_000005.9:g.58265231A>G , CM000667.1:g.58265231A>G	GRCh37
NC_000005.8:g.58300988A>G	NCBI36
NG_027957.1:g.1523695T>C
NG_027957.2:g.1559926T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000507116.6:c.*5260T>C	ENSP00000424852.1:n.*5260T>C
ENST00000340635.11:c.*5260T>C MANE Select	ENSP00000345502.6:n.*5260T>C
ENST00000340635.10:c.*5260T>C	ENSP00000345502.6:n.*5260T>C
ENST00000546160.5:c.*5260T>C	ENSP00000442734.2:n.*5260T>C
NM_001104631.1:c.*5260T>C	NP_001098101.1:n.*5260T>C
NM_001165899.1:c.*5260T>C	NP_001159371.1:n.*5260T>C
NM_001197218.1:c.*5260T>C	NP_001184147.1:n.*5260T>C
NM_001197219.1:c.*5260T>C	NP_001184148.1:n.*5260T>C
NM_001197220.1:c.*5260T>C	NP_001184149.1:n.*5260T>C
NM_001197221.1:c.*5260T>C	NP_001184150.1:n.*5260T>C
NM_001197222.1:c.*5260T>C	NP_001184151.1:n.*5260T>C
NM_001197223.1:c.*5260T>C	NP_001184152.1:n.*5260T>C
NM_006203.4:c.*5260T>C	NP_006194.2:n.*5260T>C
XM_005248537.2:c.*5260T>C	XP_005248594.1:n.*5260T>C
XM_005248538.3:c.*5260T>C	XP_005248595.1:n.*5260T>C
XM_011543469.1:c.*5260T>C	XP_011541771.1:n.*5260T>C
XM_011543470.1:c.*5260T>C	XP_011541772.1:n.*5260T>C
XM_011543471.1:c.*5260T>C	XP_011541773.1:n.*5260T>C
XM_011543472.1:c.*5260T>C	XP_011541774.1:n.*5260T>C
XM_011543473.1:c.*5260T>C	XP_011541775.1:n.*5260T>C
XM_011543474.1:c.*5260T>C	XP_011541776.1:n.*5260T>C
XM_011543475.1:c.*5260T>C	XP_011541777.1:n.*5260T>C
XM_011543476.1:c.*5260T>C	XP_011541778.1:n.*5260T>C
XM_011543477.1:c.*5260T>C	XP_011541779.1:n.*5260T>C
XM_011543478.1:c.*5260T>C	XP_011541780.1:n.*5260T>C
XM_011543479.1:c.*5260T>C	XP_011541781.1:n.*5260T>C
NM_001349241.1:c.*5260T>C	NP_001336170.1:n.*5260T>C
NM_001349242.1:c.*5260T>C	NP_001336171.1:n.*5260T>C
NM_001349243.1:c.*5260T>C	NP_001336172.1:n.*5260T>C
NM_001364599.1:c.*5260T>C	NP_001351528.1:n.*5260T>C
NM_001364603.1:c.*5260T>C	NP_001351532.1:n.*5260T>C
NM_001364604.1:c.*5260T>C	NP_001351533.1:n.*5260T>C
XM_011543470.2:c.*5260T>C	XP_011541772.1:n.*5260T>C
XM_011543471.2:c.*5260T>C	XP_011541773.1:n.*5260T>C
XM_017009565.1:c.*5260T>C	XP_016865054.1:n.*5260T>C
XM_017009566.1:c.*5260T>C	XP_016865055.1:n.*5260T>C
XM_017009567.1:c.*5260T>C	XP_016865056.1:n.*5260T>C
XM_024446110.1:c.*5260T>C	XP_024301878.1:n.*5260T>C
XM_024446112.1:c.*5260T>C	XP_024301880.1:n.*5260T>C
NM_001104631.2:c.*5260T>C MANE Select	NP_001098101.1:n.*5260T>C
NM_001165899.2:c.*5260T>C	NP_001159371.1:n.*5260T>C
NM_001197218.2:c.*5260T>C	NP_001184147.1:n.*5260T>C
NM_001197219.2:c.*5260T>C	NP_001184148.1:n.*5260T>C
NM_001197220.2:c.*5260T>C	NP_001184149.1:n.*5260T>C
NM_001197221.2:c.*5260T>C	NP_001184150.1:n.*5260T>C
NM_001197222.2:c.*5260T>C	NP_001184151.1:n.*5260T>C
NM_001197223.2:c.*5260T>C	NP_001184152.1:n.*5260T>C
NM_001349241.2:c.*5260T>C	NP_001336170.1:n.*5260T>C
NM_001349243.2:c.*5260T>C	NP_001336172.1:n.*5260T>C
NM_001349242.2:c.*5260T>C	NP_001336171.1:n.*5260T>C
NM_006203.5:c.*5260T>C	NP_006194.2:n.*5260T>C