Canonical Allele Identifier: CA1590703879
Gene: PDE6A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149896682G= , CM000667.2:g.149896682G= GRCh38
NC_000005.9:g.149276245G= , CM000667.1:g.149276245G= GRCh37
NC_000005.8:g.149256438G= NCBI36
NG_009102.1:g.53112C=

Transcript Alleles

HGVS Amino-acid change
ENST00000255266.10:c.1473+29C= MANE Select ENSP00000255266.5:n.1473+29C=
ENST00000255266.9:c.1473+29C= ENSP00000255266.5:n.1473+29C=
ENST00000508173.5:n.1478C=
ENST00000613228.1:c.1230+29C= ENSP00000478060.1:n.1230+29C=
ENST00000617647.4:c.1230+29C= ENSP00000482774.1:n.1230+29C=
NM_000440.2:c.1473+29C= NP_000431.2:n.1473+29C=
XM_011537648.1:c.1473+29C= XP_011535950.1:n.1473+29C=
XM_011537649.1:c.927+29C= XP_011535951.1:n.927+29C=
XM_011537650.1:c.588+29C= XP_011535952.1:n.588+29C=
XM_011537651.1:c.426+29C= XP_011535953.1:n.426+29C=
XM_011537652.1:c.396+29C= XP_011535954.1:n.396+29C=
XM_011537653.1:c.396+29C= XP_011535955.1:n.396+29C=
XM_011537654.1:c.396+29C= XP_011535956.1:n.396+29C=
XM_011537650.2:c.588+29C= XP_011535952.1:n.588+29C=
XM_011537651.2:c.426+29C= XP_011535953.1:n.426+29C=
XM_011537653.2:c.396+29C= XP_011535955.1:n.396+29C=
XM_011537654.2:c.396+29C= XP_011535956.1:n.396+29C=
XM_017009572.2:c.1230+29C= XP_016865061.1:n.1230+29C=
NM_000440.3:c.1473+29C= MANE Select NP_000431.2:n.1473+29C=