Canonical Allele Identifier: CA1590702429

Gene: PDE6A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149895193G= , CM000667.2:g.149895193G=	GRCh38
NC_000005.9:g.149274756G= , CM000667.1:g.149274756G=	GRCh37
NC_000005.8:g.149254949G=	NCBI36
NG_009102.1:g.54601C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255266.10:c.1718C= MANE Select	ENSP00000255266.5:p.Ser573=
ENST00000255266.9:c.1718C=	ENSP00000255266.5:p.Ser573=
ENST00000508173.5:n.1902C=
ENST00000613228.1:c.1475C=	ENSP00000478060.1:p.Ser492=
ENST00000617647.4:c.1475C=	ENSP00000482774.1:p.Ser492=
NM_000440.2:c.1718C=	NP_000431.2:p.Ser573=
XM_011537648.1:c.1718C=	XP_011535950.1:p.Ser573=
XM_011537649.1:c.1172C=	XP_011535951.1:p.Ser391=
XM_011537650.1:c.833C=	XP_011535952.1:p.Ser278=
XM_011537651.1:c.671C=	XP_011535953.1:p.Ser224=
XM_011537652.1:c.641C=	XP_011535954.1:p.Ser214=
XM_011537653.1:c.641C=	XP_011535955.1:p.Ser214=
XM_011537654.1:c.641C=	XP_011535956.1:p.Ser214=
XM_011537650.2:c.833C=	XP_011535952.1:p.Ser278=
XM_011537651.2:c.671C=	XP_011535953.1:p.Ser224=
XM_011537653.2:c.641C=	XP_011535955.1:p.Ser214=
XM_011537654.2:c.641C=	XP_011535956.1:p.Ser214=
XM_017009572.2:c.1475C=	XP_016865061.1:p.Ser492=
NM_000440.3:c.1718C= MANE Select	NP_000431.2:p.Ser573=