Canonical Allele Identifier: CA361688471
Community Standard Title: NM_000440.3(PDE6A):c.2275-1G>A
Gene: PDE6A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149866254C>T , CM000667.2:g.149866254C>T GRCh38
NC_000005.9:g.149245817C>T , CM000667.1:g.149245817C>T GRCh37
NC_000005.8:g.149226010C>T NCBI36
NG_009102.1:g.83540G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000440.3:c.2275-1G>A MANE Select NP_000431.2:n.2275-1G>A
ENST00000255266.10:c.2275-1G>A MANE Select ENSP00000255266.5:n.2275-1G>A
NM_000440.2:c.2275-1G>A NP_000431.2:n.2275-1G>A
ENST00000255266.9:c.2275-1G>A ENSP00000255266.5:n.2275-1G>A
ENST00000508173.5:n.2459-1G>A
ENST00000512670.1:n.1639G>A
ENST00000613228.1:c.2032-1G>A ENSP00000478060.1:n.2032-1G>A
ENST00000617647.4:c.2032-1G>A ENSP00000482774.1:n.2032-1G>A
XM_011537648.1:c.2275-1G>A XP_011535950.1:n.2275-1G>A
XM_011537649.1:c.1729-1G>A XP_011535951.1:n.1729-1G>A
XM_011537650.1:c.1390-1G>A XP_011535952.1:n.1390-1G>A
XM_011537650.2:c.1390-1G>A XP_011535952.1:n.1390-1G>A
XM_011537651.1:c.1228-1G>A XP_011535953.1:n.1228-1G>A
XM_011537651.2:c.1228-1G>A XP_011535953.1:n.1228-1G>A
XM_011537652.1:c.1198-1G>A XP_011535954.1:n.1198-1G>A
XM_011537653.1:c.1198-1G>A XP_011535955.1:n.1198-1G>A
XM_011537653.2:c.1198-1G>A XP_011535955.1:n.1198-1G>A
XM_011537654.1:c.1198-1G>A XP_011535956.1:n.1198-1G>A
XM_011537654.2:c.1198-1G>A XP_011535956.1:n.1198-1G>A
XM_017009572.2:c.2032-1G>A XP_016865061.1:n.2032-1G>A