Canonical Allele Identifier: CA3504420
Community Standard Title: NM_000440.3(PDE6A):c.2037G>A (p.Thr679=)
Gene: PDE6A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149883527C>T , CM000667.2:g.149883527C>T GRCh38
NC_000005.9:g.149263090C>T , CM000667.1:g.149263090C>T GRCh37
NC_000005.8:g.149243283C>T NCBI36
NG_009102.1:g.66267G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000440.3:c.2037G>A MANE Select NP_000431.2:p.Thr679=
ENST00000255266.10:c.2037G>A MANE Select ENSP00000255266.5:p.Thr679=
NM_000440.2:c.2037G>A NP_000431.2:p.Thr679=
ENST00000255266.9:c.2037G>A ENSP00000255266.5:p.Thr679=
ENST00000508173.5:n.2221G>A
ENST00000613228.1:c.1794G>A ENSP00000478060.1:p.Thr598=
ENST00000617647.4:c.1794G>A ENSP00000482774.1:p.Thr598=
XM_011537648.1:c.2037G>A XP_011535950.1:p.Thr679=
XM_011537649.1:c.1491G>A XP_011535951.1:p.Thr497=
XM_011537650.1:c.1152G>A XP_011535952.1:p.Thr384=
XM_011537650.2:c.1152G>A XP_011535952.1:p.Thr384=
XM_011537651.1:c.990G>A XP_011535953.1:p.Thr330=
XM_011537651.2:c.990G>A XP_011535953.1:p.Thr330=
XM_011537652.1:c.960G>A XP_011535954.1:p.Thr320=
XM_011537653.1:c.960G>A XP_011535955.1:p.Thr320=
XM_011537653.2:c.960G>A XP_011535955.1:p.Thr320=
XM_011537654.1:c.960G>A XP_011535956.1:p.Thr320=
XM_011537654.2:c.960G>A XP_011535956.1:p.Thr320=
XM_017009572.2:c.1794G>A XP_016865061.1:p.Thr598=