Canonical Allele Identifier: CA361695151
Gene: PDE6A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149895238T>A , CM000667.2:g.149895238T>A GRCh38
NC_000005.9:g.149274801T>A , CM000667.1:g.149274801T>A GRCh37
NC_000005.8:g.149254994T>A NCBI36
NG_009102.1:g.54556A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000255266.10:c.1673A>T MANE Select ENSP00000255266.5:p.Tyr558Phe
ENST00000255266.9:c.1673A>T ENSP00000255266.5:p.Tyr558Phe
ENST00000508173.5:n.1857A>T
ENST00000613228.1:c.1430A>T ENSP00000478060.1:p.Tyr477Phe
ENST00000617647.4:c.1430A>T ENSP00000482774.1:p.Tyr477Phe
NM_000440.2:c.1673A>T NP_000431.2:p.Tyr558Phe
XM_011537648.1:c.1673A>T XP_011535950.1:p.Tyr558Phe
XM_011537649.1:c.1127A>T XP_011535951.1:p.Tyr376Phe
XM_011537650.1:c.788A>T XP_011535952.1:p.Tyr263Phe
XM_011537651.1:c.626A>T XP_011535953.1:p.Tyr209Phe
XM_011537652.1:c.596A>T XP_011535954.1:p.Tyr199Phe
XM_011537653.1:c.596A>T XP_011535955.1:p.Tyr199Phe
XM_011537654.1:c.596A>T XP_011535956.1:p.Tyr199Phe
XM_011537650.2:c.788A>T XP_011535952.1:p.Tyr263Phe
XM_011537651.2:c.626A>T XP_011535953.1:p.Tyr209Phe
XM_011537653.2:c.596A>T XP_011535955.1:p.Tyr199Phe
XM_011537654.2:c.596A>T XP_011535956.1:p.Tyr199Phe
XM_017009572.2:c.1430A>T XP_016865061.1:p.Tyr477Phe
NM_000440.3:c.1673A>T MANE Select NP_000431.2:p.Tyr558Phe