Canonical Allele Identifier: CA812695681

Gene: PDE4D

Linked Data

• dbSNP Id: rs1201923167
• gnomAD v3: 5-60487393-TA-T
• gnomAD v4: 5-60487393-TA-T
• MyVariant Identifiers: chr5:g.59783221del (hg19) ; chr5:g.60487394del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.60487398del , CM000667.2:g.60487398del	GRCh38
NC_000005.9:g.59783225del , CM000667.1:g.59783225del	GRCh37
NC_000005.8:g.59818982del	NCBI36
NG_027957.1:g.5705del
NG_027957.2:g.41936del

Transcript Alleles

HGVS	Amino-acid change
ENST00000502484.6:c.-90+548del	ENSP00000423094.2:n.-90+548del
ENST00000505507.6:c.-213+548del	ENSP00000425910.2:n.-213+548del
ENST00000506510.6:n.70+34657del
ENST00000509355.5:n.157+548del
ENST00000511382.1:n.124+548del
ENST00000515835.2:c.-213+548del	ENSP00000424281.2:n.-213+548del
NM_001165899.1:c.-90+548del	NP_001159371.1:n.-90+548del
XM_011543472.1:c.-90+34657del	XP_011541774.1:n.-90+34657del
NM_001349241.1:c.-193+548del	NP_001336170.1:n.-193+548del
NM_001349243.1:c.-674+548del	NP_001336172.1:n.-674+548del
NM_001364599.1:c.-90+8745del	NP_001351528.1:n.-90+8745del
XM_017009566.1:c.-139+548del	XP_016865055.1:n.-139+548del
XM_024446110.1:c.-90+34657del	XP_024301878.1:n.-90+34657del
XM_024446112.1:c.-90+34657del	XP_024301880.1:n.-90+34657del
NM_001165899.2:c.-90+548del	NP_001159371.1:n.-90+548del
NM_001349241.2:c.-193+548del	NP_001336170.1:n.-193+548del
NM_001349243.2:c.-674+548del	NP_001336172.1:n.-674+548del