Canonical Allele Identifier: CA10623412
Gene: PDE6A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149860664dup , CM000667.2:g.149860664dup GRCh38
NC_000005.9:g.149240227dup , CM000667.1:g.149240227dup GRCh37
NC_000005.8:g.149220420dup NCBI36
NG_009102.1:g.89140dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000255266.10:c.*241dup MANE Select ENSP00000255266.5:n.*241dup
ENST00000255266.9:c.*241dup ENSP00000255266.5:n.*241dup
ENST00000508173.5:n.3008dup
ENST00000613228.1:c.*241dup ENSP00000478060.1:n.*241dup
ENST00000617647.4:c.*241dup ENSP00000482774.1:n.*241dup
NM_000440.2:c.*241dup NP_000431.2:n.*241dup
XM_011537648.1:c.*241dup XP_011535950.1:n.*241dup
XM_011537649.1:c.*241dup XP_011535951.1:n.*241dup
XM_011537650.1:c.*241dup XP_011535952.1:n.*241dup
XM_011537651.1:c.*241dup XP_011535953.1:n.*241dup
XM_011537652.1:c.*241dup XP_011535954.1:n.*241dup
XM_011537653.1:c.*241dup XP_011535955.1:n.*241dup
XM_011537654.1:c.*241dup XP_011535956.1:n.*241dup
XM_011537650.2:c.*241dup XP_011535952.1:n.*241dup
XM_011537651.2:c.*241dup XP_011535953.1:n.*241dup
XM_011537653.2:c.*241dup XP_011535955.1:n.*241dup
XM_011537654.2:c.*241dup XP_011535956.1:n.*241dup
XM_017009572.2:c.*241dup XP_016865061.1:n.*241dup
NM_000440.3:c.*241dup MANE Select NP_000431.2:n.*241dup