Canonical Allele Identifier: CA10620611

Gene: PDE4D

Linked Data

• ClinVar Variation Id: 353932
• ClinVar RCV Id: RCV000360677
• dbSNP Id: rs72764043
• gnomAD v2: 5-58267142-A-T
• gnomAD v3: 5-58971315-A-T
• gnomAD v4: 5-58971315-A-T
• MyVariant Identifiers: chr5:g.58267142A>T (hg19) ; chr5:g.58971315A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.58971315A>T , CM000667.2:g.58971315A>T	GRCh38
NC_000005.9:g.58267142A>T , CM000667.1:g.58267142A>T	GRCh37
NC_000005.8:g.58302899A>T	NCBI36
NG_027957.1:g.1521784T>A
NG_027957.2:g.1558015T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000507116.6:c.*3349T>A	ENSP00000424852.1:n.*3349T>A
ENST00000340635.11:c.*3349T>A MANE Select	ENSP00000345502.6:n.*3349T>A
ENST00000636120.1:c.*3349T>A	ENSP00000490821.1:n.*3349T>A
ENST00000340635.10:c.*3349T>A	ENSP00000345502.6:n.*3349T>A
ENST00000546160.5:c.*3349T>A	ENSP00000442734.2:n.*3349T>A
NM_001104631.1:c.*3349T>A	NP_001098101.1:n.*3349T>A
NM_001165899.1:c.*3349T>A	NP_001159371.1:n.*3349T>A
NM_001197218.1:c.*3349T>A	NP_001184147.1:n.*3349T>A
NM_001197219.1:c.*3349T>A	NP_001184148.1:n.*3349T>A
NM_001197220.1:c.*3349T>A	NP_001184149.1:n.*3349T>A
NM_001197221.1:c.*3349T>A	NP_001184150.1:n.*3349T>A
NM_001197222.1:c.*3349T>A	NP_001184151.1:n.*3349T>A
NM_001197223.1:c.*3349T>A	NP_001184152.1:n.*3349T>A
NM_006203.4:c.*3349T>A	NP_006194.2:n.*3349T>A
XM_005248537.2:c.*3349T>A	XP_005248594.1:n.*3349T>A
XM_005248538.3:c.*3349T>A	XP_005248595.1:n.*3349T>A
XM_011543469.1:c.*3349T>A	XP_011541771.1:n.*3349T>A
XM_011543470.1:c.*3349T>A	XP_011541772.1:n.*3349T>A
XM_011543471.1:c.*3349T>A	XP_011541773.1:n.*3349T>A
XM_011543472.1:c.*3349T>A	XP_011541774.1:n.*3349T>A
XM_011543473.1:c.*3349T>A	XP_011541775.1:n.*3349T>A
XM_011543474.1:c.*3349T>A	XP_011541776.1:n.*3349T>A
XM_011543475.1:c.*3349T>A	XP_011541777.1:n.*3349T>A
XM_011543476.1:c.*3349T>A	XP_011541778.1:n.*3349T>A
XM_011543477.1:c.*3349T>A	XP_011541779.1:n.*3349T>A
XM_011543478.1:c.*3349T>A	XP_011541780.1:n.*3349T>A
XM_011543479.1:c.*3349T>A	XP_011541781.1:n.*3349T>A
NM_001349241.1:c.*3349T>A	NP_001336170.1:n.*3349T>A
NM_001349242.1:c.*3349T>A	NP_001336171.1:n.*3349T>A
NM_001349243.1:c.*3349T>A	NP_001336172.1:n.*3349T>A
NM_001364599.1:c.*3349T>A	NP_001351528.1:n.*3349T>A
NM_001364603.1:c.*3349T>A	NP_001351532.1:n.*3349T>A
NM_001364604.1:c.*3349T>A	NP_001351533.1:n.*3349T>A
XM_011543470.2:c.*3349T>A	XP_011541772.1:n.*3349T>A
XM_011543471.2:c.*3349T>A	XP_011541773.1:n.*3349T>A
XM_017009565.1:c.*3349T>A	XP_016865054.1:n.*3349T>A
XM_017009566.1:c.*3349T>A	XP_016865055.1:n.*3349T>A
XM_017009567.1:c.*3349T>A	XP_016865056.1:n.*3349T>A
XM_024446110.1:c.*3349T>A	XP_024301878.1:n.*3349T>A
XM_024446112.1:c.*3349T>A	XP_024301880.1:n.*3349T>A
NM_001104631.2:c.*3349T>A MANE Select	NP_001098101.1:n.*3349T>A
NM_001165899.2:c.*3349T>A	NP_001159371.1:n.*3349T>A
NM_001197218.2:c.*3349T>A	NP_001184147.1:n.*3349T>A
NM_001197219.2:c.*3349T>A	NP_001184148.1:n.*3349T>A
NM_001197220.2:c.*3349T>A	NP_001184149.1:n.*3349T>A
NM_001197221.2:c.*3349T>A	NP_001184150.1:n.*3349T>A
NM_001197222.2:c.*3349T>A	NP_001184151.1:n.*3349T>A
NM_001197223.2:c.*3349T>A	NP_001184152.1:n.*3349T>A
NM_001349241.2:c.*3349T>A	NP_001336170.1:n.*3349T>A
NM_001349243.2:c.*3349T>A	NP_001336172.1:n.*3349T>A
NM_001349242.2:c.*3349T>A	NP_001336171.1:n.*3349T>A
NM_006203.5:c.*3349T>A	NP_006194.2:n.*3349T>A