Canonical Allele Identifier: CA361695595

Gene: PDE6A

Linked Data

• MyVariant Identifiers: chr5:g.149276063T>A (hg19) ; chr5:g.149896500T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149896500T>A , CM000667.2:g.149896500T>A	GRCh38
NC_000005.9:g.149276063T>A , CM000667.1:g.149276063T>A	GRCh37
NC_000005.8:g.149256256T>A	NCBI36
NG_009102.1:g.53294A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255266.10:c.1476A>T MANE Select	ENSP00000255266.5:p.Gln492His
ENST00000255266.9:c.1476A>T	ENSP00000255266.5:p.Gln492His
ENST00000508173.5:n.1660A>T
ENST00000613228.1:c.1233A>T	ENSP00000478060.1:p.Gln411His
ENST00000617647.4:c.1233A>T	ENSP00000482774.1:p.Gln411His
NM_000440.2:c.1476A>T	NP_000431.2:p.Gln492His
XM_011537648.1:c.1476A>T	XP_011535950.1:p.Gln492His
XM_011537649.1:c.930A>T	XP_011535951.1:p.Gln310His
XM_011537650.1:c.591A>T	XP_011535952.1:p.Gln197His
XM_011537651.1:c.429A>T	XP_011535953.1:p.Gln143His
XM_011537652.1:c.399A>T	XP_011535954.1:p.Gln133His
XM_011537653.1:c.399A>T	XP_011535955.1:p.Gln133His
XM_011537654.1:c.399A>T	XP_011535956.1:p.Gln133His
XM_011537650.2:c.591A>T	XP_011535952.1:p.Gln197His
XM_011537651.2:c.429A>T	XP_011535953.1:p.Gln143His
XM_011537653.2:c.399A>T	XP_011535955.1:p.Gln133His
XM_011537654.2:c.399A>T	XP_011535956.1:p.Gln133His
XM_017009572.2:c.1233A>T	XP_016865061.1:p.Gln411His
NM_000440.3:c.1476A>T MANE Select	NP_000431.2:p.Gln492His