Canonical Allele Identifier: CA631735094

Gene: PDE4A

Linked Data

• dbSNP Id: rs775295718
• gnomAD v2: 19-10568546-C-T
• gnomAD v4: 19-10457870-C-T
• MyVariant Identifiers: chr19:g.10568546C>T (hg19) ; chr19:g.10457870C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10457870C>T , CM000681.2:g.10457870C>T	GRCh38
NC_000019.9:g.10568546C>T , CM000681.1:g.10568546C>T	GRCh37
NC_000019.8:g.10429546C>T	NCBI36
NG_029594.1:g.46098C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000380702.7:c.878-9C>T MANE Select	ENSP00000370078.3:n.878-9C>T
ENST00000293683.9:c.800-9C>T	ENSP00000293683.4:n.800-9C>T
ENST00000344979.7:c.161-9C>T	ENSP00000341007.2:n.161-9C>T
ENST00000380702.6:c.878-9C>T	ENSP00000370078.3:n.878-9C>T
ENST00000440014.6:c.695-9C>T	ENSP00000394754.1:n.695-9C>T
ENST00000586275.1:n.141-9C>T
ENST00000589073.1:c.160+2948C>T	ENSP00000465792.1:n.160+2948C>T
ENST00000591971.5:c.206-9C>T	ENSP00000467137.1:n.206-9C>T
ENST00000592685.5:c.812-9C>T	ENSP00000468507.1:n.812-9C>T
NM_001111307.1:c.878-9C>T	NP_001104777.1:n.878-9C>T
NM_001111308.1:c.800-9C>T	NP_001104778.1:n.800-9C>T
NM_001111309.1:c.695-9C>T	NP_001104779.1:n.695-9C>T
NM_001243121.1:c.812-9C>T	NP_001230050.1:n.812-9C>T
NM_006202.2:c.161-9C>T	NP_006193.1:n.161-9C>T
XM_005259933.2:c.-35-9C>T	XP_005259990.1:n.-35-9C>T
XM_011528054.1:c.812-9C>T	XP_011526356.1:n.812-9C>T
XM_011528055.1:c.878-9C>T	XP_011526357.1:n.878-9C>T
XM_011528055.3:c.878-9C>T	XP_011526357.1:n.878-9C>T
XM_017026865.2:c.875-9C>T	XP_016882354.1:n.875-9C>T
XM_024451534.1:c.-35-9C>T	XP_024307302.1:n.-35-9C>T
NM_001111307.2:c.878-9C>T MANE Select	NP_001104777.1:n.878-9C>T
NM_006202.3:c.161-9C>T	NP_006193.1:n.161-9C>T
NM_001243121.2:c.812-9C>T	NP_001230050.1:n.812-9C>T