Canonical Allele Identifier: CA119456619

Gene: PDE4D

Linked Data

• dbSNP Id: rs746287639
• gnomAD v3: 5-60413817-CAA-C
• gnomAD v4: 5-60413817-CAA-C
• MyVariant Identifiers: chr5:g.59709645_59709646del (hg19) ; chr5:g.60413818_60413819del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.60413819_60413820del , CM000667.2:g.60413819_60413820del	GRCh38
NC_000005.9:g.59709646_59709647del , CM000667.1:g.59709646_59709647del	GRCh37
NC_000005.8:g.59745403_59745404del	NCBI36
NG_027957.1:g.79280_79281del
NG_027957.2:g.115511_115512del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502484.6:c.-90+74123_-90+74124del	ENSP00000423094.2:n.-90+74123_-90+74124del
ENST00000505507.6:c.-213+74123_-213+74124del	ENSP00000425910.2:n.-213+74123_-213+74124del
ENST00000506024.5:n.71+34818_71+34819del
ENST00000506510.6:n.70+108232_70+108233del
ENST00000509355.5:n.157+74123_157+74124del
ENST00000511382.1:n.124+74123_124+74124del
ENST00000515835.2:c.-213+74123_-213+74124del	ENSP00000424281.2:n.-213+74123_-213+74124del
NM_001165899.1:c.-90+74123_-90+74124del	NP_001159371.1:n.-90+74123_-90+74124del
XM_011543472.1:c.-90+108232_-90+108233del	XP_011541774.1:n.-90+108232_-90+108233del
XM_011543473.1:c.-90+34818_-90+34819del	XP_011541775.1:n.-90+34818_-90+34819del
NM_001349241.1:c.-193+74123_-193+74124del	NP_001336170.1:n.-193+74123_-193+74124del
NM_001349243.1:c.-674+74123_-674+74124del	NP_001336172.1:n.-674+74123_-674+74124del
NM_001364599.1:c.-90+82320_-90+82321del	NP_001351528.1:n.-90+82320_-90+82321del
XM_017009566.1:c.-139+74123_-139+74124del	XP_016865055.1:n.-139+74123_-139+74124del
XM_024446110.1:c.-90+108232_-90+108233del	XP_024301878.1:n.-90+108232_-90+108233del
XM_024446112.1:c.-90+108232_-90+108233del	XP_024301880.1:n.-90+108232_-90+108233del
NM_001165899.2:c.-90+74123_-90+74124del	NP_001159371.1:n.-90+74123_-90+74124del
NM_001349241.2:c.-193+74123_-193+74124del	NP_001336170.1:n.-193+74123_-193+74124del
NM_001349243.2:c.-674+74123_-674+74124del	NP_001336172.1:n.-674+74123_-674+74124del