Canonical Allele Identifier: CA1488959092
Gene: SEPTIN7P14 HGNC NCBI
PDE5A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119501164A= , CM000666.2:g.119501164A= GRCh38
NC_000004.11:g.120422319A= , CM000666.1:g.120422319A= GRCh37
NC_000004.10:g.120641767A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000508519.6:n.931+6641A= (SEPTIN7P14)
ENST00000685525.1:n.1042+3261A= (SEPTIN7P14)
ENST00000685974.1:n.939+3261A= (SEPTIN7P14)
ENST00000686202.1:n.892+6641A= (SEPTIN7P14)
ENST00000688315.1:n.1003+3261A= (SEPTIN7P14)
ENST00000688480.1:n.998+3261A= (SEPTIN7P14)
ENST00000690731.1:n.939+3261A= (SEPTIN7P14)
ENST00000692409.1:n.939+3261A= (SEPTIN7P14)
ENST00000692642.1:n.1012+3261A= (SEPTIN7P14)
ENST00000692945.1:n.984+3261A= (SEPTIN7P14)
ENST00000354960.8:c.2490+6T= (PDE5A) MANE Select ENSP00000347046.3:n.2490+6T=
ENST00000264805.9:c.2364+6T= (PDE5A) ENSP00000264805.5:n.2364+6T=
ENST00000354960.7:c.2490+6T= (PDE5A) ENSP00000347046.3:n.2490+6T=
ENST00000394439.5:c.2334+6T= (PDE5A) ENSP00000377957.1:n.2334+6T=
ENST00000498873.5:n.364+3261A= (SEPTIN7P14)
ENST00000503412.1:c.551T= (PDE5A)
ENST00000510844.5:n.191+3261A= (SEPTIN7P14)
NM_001083.3:c.2490+6T= (PDE5A) NP_001074.2:n.2490+6T=
NM_033430.2:c.2364+6T= (PDE5A) NP_236914.2:n.2364+6T=
NM_033437.3:c.2334+6T= (PDE5A) NP_246273.2:n.2334+6T=
NM_001083.4:c.2490+6T= (PDE5A) MANE Select NP_001074.2:n.2490+6T=
NM_033430.3:c.2364+6T= (PDE5A) NP_236914.2:n.2364+6T=
NM_033437.4:c.2334+6T= (PDE5A) NP_246273.2:n.2334+6T=