Canonical Allele Identifier: CA361696965
Community Standard Title: NM_000440.3(PDE6A):c.1166C>T (p.Pro389Leu)
Gene: PDE6A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149899472G>A , CM000667.2:g.149899472G>A GRCh38
NC_000005.9:g.149279035G>A , CM000667.1:g.149279035G>A GRCh37
NC_000005.8:g.149259228G>A NCBI36
NG_009102.1:g.50322C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000440.3:c.1166C>T MANE Select NP_000431.2:p.Pro389Leu
ENST00000255266.10:c.1166C>T MANE Select ENSP00000255266.5:p.Pro389Leu
NM_000440.2:c.1166C>T NP_000431.2:p.Pro389Leu
ENST00000255266.9:c.1166C>T ENSP00000255266.5:p.Pro389Leu
ENST00000508173.5:n.1286C>T
ENST00000613228.1:c.923C>T ENSP00000478060.1:p.Pro308Leu
ENST00000617647.4:c.923C>T ENSP00000482774.1:p.Pro308Leu
XM_011537648.1:c.1166C>T XP_011535950.1:p.Pro389Leu
XM_011537649.1:c.620C>T XP_011535951.1:p.Pro207Leu
XM_011537650.1:c.281C>T XP_011535952.1:p.Pro94Leu
XM_011537650.2:c.281C>T XP_011535952.1:p.Pro94Leu
XM_011537651.1:c.119C>T XP_011535953.1:p.Pro40Leu
XM_011537651.2:c.119C>T XP_011535953.1:p.Pro40Leu
XM_011537652.1:c.89C>T XP_011535954.1:p.Pro30Leu
XM_011537653.1:c.89C>T XP_011535955.1:p.Pro30Leu
XM_011537653.2:c.89C>T XP_011535955.1:p.Pro30Leu
XM_011537654.1:c.89C>T XP_011535956.1:p.Pro30Leu
XM_011537654.2:c.89C>T XP_011535956.1:p.Pro30Leu
XM_017009572.2:c.923C>T XP_016865061.1:p.Pro308Leu