Canonical Allele Identifier: CA3504950
Community Standard Title: NM_000440.3(PDE6A):c.765C>T (p.Ile255=)
Gene: PDE6A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149931121G>A , CM000667.2:g.149931121G>A GRCh38
NC_000005.9:g.149310684G>A , CM000667.1:g.149310684G>A GRCh37
NC_000005.8:g.149290877G>A NCBI36
NG_009102.1:g.18673C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000440.3:c.765C>T MANE Select NP_000431.2:p.Ile255=
ENST00000255266.10:c.765C>T MANE Select ENSP00000255266.5:p.Ile255=
NM_000440.2:c.765C>T NP_000431.2:p.Ile255=
ENST00000255266.9:c.765C>T ENSP00000255266.5:p.Ile255=
ENST00000508173.5:n.885C>T
ENST00000613228.1:c.522C>T ENSP00000478060.1:p.Ile174=
ENST00000617647.4:c.522C>T ENSP00000482774.1:p.Ile174=
XM_011537648.1:c.765C>T XP_011535950.1:p.Ile255=
XM_011537649.1:c.219C>T XP_011535951.1:p.Ile73=
XM_017009572.2:c.522C>T XP_016865061.1:p.Ile174=