Canonical Allele Identifier: CA361695165
Gene: PDE6A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149895244A>T , CM000667.2:g.149895244A>T GRCh38
NC_000005.9:g.149274807A>T , CM000667.1:g.149274807A>T GRCh37
NC_000005.8:g.149255000A>T NCBI36
NG_009102.1:g.54550T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000255266.10:c.1667T>A MANE Select ENSP00000255266.5:p.Ile556Asn
ENST00000255266.9:c.1667T>A ENSP00000255266.5:p.Ile556Asn
ENST00000508173.5:n.1851T>A
ENST00000613228.1:c.1424T>A ENSP00000478060.1:p.Ile475Asn
ENST00000617647.4:c.1424T>A ENSP00000482774.1:p.Ile475Asn
NM_000440.2:c.1667T>A NP_000431.2:p.Ile556Asn
XM_011537648.1:c.1667T>A XP_011535950.1:p.Ile556Asn
XM_011537649.1:c.1121T>A XP_011535951.1:p.Ile374Asn
XM_011537650.1:c.782T>A XP_011535952.1:p.Ile261Asn
XM_011537651.1:c.620T>A XP_011535953.1:p.Ile207Asn
XM_011537652.1:c.590T>A XP_011535954.1:p.Ile197Asn
XM_011537653.1:c.590T>A XP_011535955.1:p.Ile197Asn
XM_011537654.1:c.590T>A XP_011535956.1:p.Ile197Asn
XM_011537650.2:c.782T>A XP_011535952.1:p.Ile261Asn
XM_011537651.2:c.620T>A XP_011535953.1:p.Ile207Asn
XM_011537653.2:c.590T>A XP_011535955.1:p.Ile197Asn
XM_011537654.2:c.590T>A XP_011535956.1:p.Ile197Asn
XM_017009572.2:c.1424T>A XP_016865061.1:p.Ile475Asn
NM_000440.3:c.1667T>A MANE Select NP_000431.2:p.Ile556Asn