Canonical Allele Identifier: CA1590705199
Gene: PDE6A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149898410_149898412delinsCTA , CM000667.2:g.149898410_149898412delinsCTA GRCh38
NC_000005.9:g.149277973_149277975delinsCTA , CM000667.1:g.149277973_149277975delinsCTA GRCh37
NC_000005.8:g.149258166_149258168delinsCTA NCBI36
NG_009102.1:g.51382_51384delinsTAG

Transcript Alleles

HGVS Amino-acid change
ENST00000255266.10:c.1358_1360delinsTAG MANE Select ENSP00000255266.5:p.Ile453=
ENST00000255266.9:c.1358_1360delinsTAG ENSP00000255266.5:p.Ile453=
ENST00000508173.5:n.1383+963_1383+965delinsTAG
ENST00000613228.1:c.1115_1117delinsTAG ENSP00000478060.1:p.Ile372=
ENST00000617647.4:c.1115_1117delinsTAG ENSP00000482774.1:p.Ile372=
NM_000440.2:c.1358_1360delinsTAG NP_000431.2:p.Ile453=
XM_011537648.1:c.1358_1360delinsTAG XP_011535950.1:p.Ile453=
XM_011537649.1:c.812_814delinsTAG XP_011535951.1:p.Ile271=
XM_011537650.1:c.473_475delinsTAG XP_011535952.1:p.Ile158=
XM_011537651.1:c.311_313delinsTAG XP_011535953.1:p.Ile104=
XM_011537652.1:c.281_283delinsTAG XP_011535954.1:p.Ile94=
XM_011537653.1:c.281_283delinsTAG XP_011535955.1:p.Ile94=
XM_011537654.1:c.281_283delinsTAG XP_011535956.1:p.Ile94=
XM_011537650.2:c.473_475delinsTAG XP_011535952.1:p.Ile158=
XM_011537651.2:c.311_313delinsTAG XP_011535953.1:p.Ile104=
XM_011537653.2:c.281_283delinsTAG XP_011535955.1:p.Ile94=
XM_011537654.2:c.281_283delinsTAG XP_011535956.1:p.Ile94=
XM_017009572.2:c.1115_1117delinsTAG XP_016865061.1:p.Ile372=
NM_000440.3:c.1358_1360delinsTAG MANE Select NP_000431.2:p.Ile453=