Canonical Allele Identifier: CA2581485129

Gene: PDE4D

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.59801097C>G , CM000667.2:g.59801097C>G	GRCh38
NC_000005.9:g.59096923C>G , CM000667.1:g.59096923C>G	GRCh37
NC_000005.8:g.59132680C>G	NCBI36
NG_027957.1:g.692003G>C
NG_027957.2:g.728233G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340635.11:c.455+92071G>C MANE Select	ENSP00000345502.6:n.455+92071G>C
ENST00000340635.10:c.455+92071G>C	ENSP00000345502.6:n.455+92071G>C
ENST00000405053.7:n.118+92071G>C
ENST00000502484.6:c.272+187391G>C	ENSP00000423094.2:n.272+187391G>C
ENST00000512069.6:n.217+187391G>C
ENST00000514231.1:n.146-3965G>C
NM_001104631.1:c.455+92071G>C	NP_001098101.1:n.455+92071G>C
NM_001165899.1:c.272+187391G>C	NP_001159371.1:n.272+187391G>C
XM_011543469.1:c.419+187391G>C	XP_011541771.1:n.419+187391G>C
XM_011543470.1:c.419+187391G>C	XP_011541772.1:n.419+187391G>C
XM_011543471.1:c.272+187391G>C	XP_011541773.1:n.272+187391G>C
XM_011543472.1:c.272+187391G>C	XP_011541774.1:n.272+187391G>C
XM_011543473.1:c.272+187391G>C	XP_011541775.1:n.272+187391G>C
XM_011543474.1:c.242+187391G>C	XP_011541776.1:n.242+187391G>C
XR_948357.1:n.172+13208C>G
NM_001349241.1:c.242+187391G>C	NP_001336170.1:n.242+187391G>C
NM_001349243.1:c.-240+187391G>C	NP_001336172.1:n.-240+187391G>C
NM_001364599.1:c.272+187391G>C	NP_001351528.1:n.272+187391G>C
NM_001364600.1:c.272+187391G>C	NP_001351529.1:n.272+187391G>C
XM_011543470.2:c.419+187391G>C	XP_011541772.1:n.419+187391G>C
XM_011543471.2:c.272+187391G>C	XP_011541773.1:n.272+187391G>C
XM_017009565.1:c.419+187391G>C	XP_016865054.1:n.419+187391G>C
XM_017009566.1:c.272+187391G>C	XP_016865055.1:n.272+187391G>C
XM_017009567.1:c.257+187391G>C	XP_016865056.1:n.257+187391G>C
XM_024446110.1:c.419+187391G>C	XP_024301878.1:n.419+187391G>C
XM_024446112.1:c.272+187391G>C	XP_024301880.1:n.272+187391G>C
NM_001104631.2:c.455+92071G>C MANE Select	NP_001098101.1:n.455+92071G>C
NM_001165899.2:c.272+187391G>C	NP_001159371.1:n.272+187391G>C
NM_001349241.2:c.242+187391G>C	NP_001336170.1:n.242+187391G>C
NM_001349243.2:c.-240+187391G>C	NP_001336172.1:n.-240+187391G>C
NM_001364600.2:c.272+187391G>C	NP_001351529.1:n.272+187391G>C