Canonical Allele Identifier: CA129067116
Gene: PDE6A HGNC NCBI

Linked Data

dbSNP Id: rs1033465614

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149895247T>G , CM000667.2:g.149895247T>G GRCh38
NC_000005.9:g.149274810T>G , CM000667.1:g.149274810T>G GRCh37
NC_000005.8:g.149255003T>G NCBI36
NG_009102.1:g.54547A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000255266.10:c.1664A>C MANE Select ENSP00000255266.5:p.Lys555Thr
ENST00000255266.9:c.1664A>C ENSP00000255266.5:p.Lys555Thr
ENST00000508173.5:n.1848A>C
ENST00000613228.1:c.1421A>C ENSP00000478060.1:p.Lys474Thr
ENST00000617647.4:c.1421A>C ENSP00000482774.1:p.Lys474Thr
NM_000440.2:c.1664A>C NP_000431.2:p.Lys555Thr
XM_011537648.1:c.1664A>C XP_011535950.1:p.Lys555Thr
XM_011537649.1:c.1118A>C XP_011535951.1:p.Lys373Thr
XM_011537650.1:c.779A>C XP_011535952.1:p.Lys260Thr
XM_011537651.1:c.617A>C XP_011535953.1:p.Lys206Thr
XM_011537652.1:c.587A>C XP_011535954.1:p.Lys196Thr
XM_011537653.1:c.587A>C XP_011535955.1:p.Lys196Thr
XM_011537654.1:c.587A>C XP_011535956.1:p.Lys196Thr
XM_011537650.2:c.779A>C XP_011535952.1:p.Lys260Thr
XM_011537651.2:c.617A>C XP_011535953.1:p.Lys206Thr
XM_011537653.2:c.587A>C XP_011535955.1:p.Lys196Thr
XM_011537654.2:c.587A>C XP_011535956.1:p.Lys196Thr
XM_017009572.2:c.1421A>C XP_016865061.1:p.Lys474Thr
NM_000440.3:c.1664A>C MANE Select NP_000431.2:p.Lys555Thr