Canonical Allele Identifier: CA361695149
Community Standard Title: NM_000440.3(PDE6A):c.1674C>G (p.Tyr558Ter)
Gene: PDE6A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149895237G>C , CM000667.2:g.149895237G>C GRCh38
NC_000005.9:g.149274800G>C , CM000667.1:g.149274800G>C GRCh37
NC_000005.8:g.149254993G>C NCBI36
NG_009102.1:g.54557C>G

Transcript Alleles

HGVS Amino-acid Change
NM_000440.3:c.1674C>G MANE Select NP_000431.2:p.Tyr558Ter
ENST00000255266.10:c.1674C>G MANE Select ENSP00000255266.5:p.Tyr558Ter
NM_000440.2:c.1674C>G NP_000431.2:p.Tyr558Ter
ENST00000255266.9:c.1674C>G ENSP00000255266.5:p.Tyr558Ter
ENST00000508173.5:n.1858C>G
ENST00000613228.1:c.1431C>G ENSP00000478060.1:p.Tyr477Ter
ENST00000617647.4:c.1431C>G ENSP00000482774.1:p.Tyr477Ter
XM_011537648.1:c.1674C>G XP_011535950.1:p.Tyr558Ter
XM_011537649.1:c.1128C>G XP_011535951.1:p.Tyr376Ter
XM_011537650.1:c.789C>G XP_011535952.1:p.Tyr263Ter
XM_011537650.2:c.789C>G XP_011535952.1:p.Tyr263Ter
XM_011537651.1:c.627C>G XP_011535953.1:p.Tyr209Ter
XM_011537651.2:c.627C>G XP_011535953.1:p.Tyr209Ter
XM_011537652.1:c.597C>G XP_011535954.1:p.Tyr199Ter
XM_011537653.1:c.597C>G XP_011535955.1:p.Tyr199Ter
XM_011537653.2:c.597C>G XP_011535955.1:p.Tyr199Ter
XM_011537654.1:c.597C>G XP_011535956.1:p.Tyr199Ter
XM_011537654.2:c.597C>G XP_011535956.1:p.Tyr199Ter
XM_017009572.2:c.1431C>G XP_016865061.1:p.Tyr477Ter