Canonical Allele Identifier: CA1549802355

Gene: PDE4D

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.60487252A= , CM000667.2:g.60487252A=	GRCh38
NC_000005.9:g.59783079A= , CM000667.1:g.59783079A=	GRCh37
NC_000005.8:g.59818836A=	NCBI36
NG_027957.1:g.5847T=
NG_027957.2:g.42078T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502484.6:c.-90+690T=	ENSP00000423094.2:n.-90+690T=
ENST00000505507.6:c.-213+690T=	ENSP00000425910.2:n.-213+690T=
ENST00000506510.6:n.70+34799T=
ENST00000509355.5:n.157+690T=
ENST00000511382.1:n.124+690T=
ENST00000515835.2:c.-213+690T=	ENSP00000424281.2:n.-213+690T=
NM_001165899.1:c.-90+690T=	NP_001159371.1:n.-90+690T=
XM_011543472.1:c.-90+34799T=	XP_011541774.1:n.-90+34799T=
NM_001349241.1:c.-193+690T=	NP_001336170.1:n.-193+690T=
NM_001349243.1:c.-674+690T=	NP_001336172.1:n.-674+690T=
NM_001364599.1:c.-90+8887T=	NP_001351528.1:n.-90+8887T=
XM_017009566.1:c.-139+690T=	XP_016865055.1:n.-139+690T=
XM_024446110.1:c.-90+34799T=	XP_024301878.1:n.-90+34799T=
XM_024446112.1:c.-90+34799T=	XP_024301880.1:n.-90+34799T=
NM_001165899.2:c.-90+690T=	NP_001159371.1:n.-90+690T=
NM_001349241.2:c.-193+690T=	NP_001336170.1:n.-193+690T=
NM_001349243.2:c.-674+690T=	NP_001336172.1:n.-674+690T=