Canonical Allele Identifier: CA119456644

Gene: PDE4D

Linked Data

• dbSNP Id: rs958761810
• MyVariant Identifiers: chr5:g.59709778A>G (hg19) ; chr5:g.60413951A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.60413951A>G , CM000667.2:g.60413951A>G	GRCh38
NC_000005.9:g.59709778A>G , CM000667.1:g.59709778A>G	GRCh37
NC_000005.8:g.59745535A>G	NCBI36
NG_027957.1:g.79148T>C
NG_027957.2:g.115379T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000502484.6:c.-90+73991T>C	ENSP00000423094.2:n.-90+73991T>C
ENST00000505507.6:c.-213+73991T>C	ENSP00000425910.2:n.-213+73991T>C
ENST00000506024.5:n.71+34686T>C
ENST00000506510.6:n.70+108100T>C
ENST00000509355.5:n.157+73991T>C
ENST00000511382.1:n.124+73991T>C
ENST00000515835.2:c.-213+73991T>C	ENSP00000424281.2:n.-213+73991T>C
NM_001165899.1:c.-90+73991T>C	NP_001159371.1:n.-90+73991T>C
XM_011543472.1:c.-90+108100T>C	XP_011541774.1:n.-90+108100T>C
XM_011543473.1:c.-90+34686T>C	XP_011541775.1:n.-90+34686T>C
NM_001349241.1:c.-193+73991T>C	NP_001336170.1:n.-193+73991T>C
NM_001349243.1:c.-674+73991T>C	NP_001336172.1:n.-674+73991T>C
NM_001364599.1:c.-90+82188T>C	NP_001351528.1:n.-90+82188T>C
XM_017009566.1:c.-139+73991T>C	XP_016865055.1:n.-139+73991T>C
XM_024446110.1:c.-90+108100T>C	XP_024301878.1:n.-90+108100T>C
XM_024446112.1:c.-90+108100T>C	XP_024301880.1:n.-90+108100T>C
NM_001165899.2:c.-90+73991T>C	NP_001159371.1:n.-90+73991T>C
NM_001349241.2:c.-193+73991T>C	NP_001336170.1:n.-193+73991T>C
NM_001349243.2:c.-674+73991T>C	NP_001336172.1:n.-674+73991T>C