Canonical Allele Identifier: CA119473809

Gene: PDE4D

Linked Data

• dbSNP Id: rs375237198
• MyVariant Identifiers: chr5:g.59782988T>C (hg19) ; chr5:g.60487161T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.60487161T>C , CM000667.2:g.60487161T>C	GRCh38
NC_000005.9:g.59782988T>C , CM000667.1:g.59782988T>C	GRCh37
NC_000005.8:g.59818745T>C	NCBI36
NG_027957.1:g.5938A>G
NG_027957.2:g.42169A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502484.6:c.-90+781A>G	ENSP00000423094.2:n.-90+781A>G
ENST00000505507.6:c.-213+781A>G	ENSP00000425910.2:n.-213+781A>G
ENST00000506510.6:n.70+34890A>G
ENST00000509355.5:n.157+781A>G
ENST00000511382.1:n.124+781A>G
ENST00000515835.2:c.-213+781A>G	ENSP00000424281.2:n.-213+781A>G
NM_001165899.1:c.-90+781A>G	NP_001159371.1:n.-90+781A>G
XM_011543472.1:c.-90+34890A>G	XP_011541774.1:n.-90+34890A>G
NM_001349241.1:c.-193+781A>G	NP_001336170.1:n.-193+781A>G
NM_001349243.1:c.-674+781A>G	NP_001336172.1:n.-674+781A>G
NM_001364599.1:c.-90+8978A>G	NP_001351528.1:n.-90+8978A>G
XM_017009566.1:c.-139+781A>G	XP_016865055.1:n.-139+781A>G
XM_024446110.1:c.-90+34890A>G	XP_024301878.1:n.-90+34890A>G
XM_024446112.1:c.-90+34890A>G	XP_024301880.1:n.-90+34890A>G
NM_001165899.2:c.-90+781A>G	NP_001159371.1:n.-90+781A>G
NM_001349241.2:c.-193+781A>G	NP_001336170.1:n.-193+781A>G
NM_001349243.2:c.-674+781A>G	NP_001336172.1:n.-674+781A>G