Canonical Allele Identifier: CA119456628

Gene: PDE4D

Linked Data

• dbSNP Id: rs1046601385
• MyVariant Identifiers: chr5:g.59709693C>A (hg19) ; chr5:g.60413866C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.60413866C>A , CM000667.2:g.60413866C>A	GRCh38
NC_000005.9:g.59709693C>A , CM000667.1:g.59709693C>A	GRCh37
NC_000005.8:g.59745450C>A	NCBI36
NG_027957.1:g.79233G>T
NG_027957.2:g.115464G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000502484.6:c.-90+74076G>T	ENSP00000423094.2:n.-90+74076G>T
ENST00000505507.6:c.-213+74076G>T	ENSP00000425910.2:n.-213+74076G>T
ENST00000506024.5:n.71+34771G>T
ENST00000506510.6:n.70+108185G>T
ENST00000509355.5:n.157+74076G>T
ENST00000511382.1:n.124+74076G>T
ENST00000515835.2:c.-213+74076G>T	ENSP00000424281.2:n.-213+74076G>T
NM_001165899.1:c.-90+74076G>T	NP_001159371.1:n.-90+74076G>T
XM_011543472.1:c.-90+108185G>T	XP_011541774.1:n.-90+108185G>T
XM_011543473.1:c.-90+34771G>T	XP_011541775.1:n.-90+34771G>T
NM_001349241.1:c.-193+74076G>T	NP_001336170.1:n.-193+74076G>T
NM_001349243.1:c.-674+74076G>T	NP_001336172.1:n.-674+74076G>T
NM_001364599.1:c.-90+82273G>T	NP_001351528.1:n.-90+82273G>T
XM_017009566.1:c.-139+74076G>T	XP_016865055.1:n.-139+74076G>T
XM_024446110.1:c.-90+108185G>T	XP_024301878.1:n.-90+108185G>T
XM_024446112.1:c.-90+108185G>T	XP_024301880.1:n.-90+108185G>T
NM_001165899.2:c.-90+74076G>T	NP_001159371.1:n.-90+74076G>T
NM_001349241.2:c.-193+74076G>T	NP_001336170.1:n.-193+74076G>T
NM_001349243.2:c.-674+74076G>T	NP_001336172.1:n.-674+74076G>T