Canonical Allele Identifier: CA2675941466

Gene: PDE6A

Linked Data

• gnomAD v4: 5-149896681-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149896685del , CM000667.2:g.149896685del	GRCh38
NC_000005.9:g.149276248del , CM000667.1:g.149276248del	GRCh37
NC_000005.8:g.149256441del	NCBI36
NG_009102.1:g.53112del

Transcript Alleles

HGVS	Amino-acid change
ENST00000255266.10:c.1473+29del MANE Select	ENSP00000255266.5:n.1473+29del
ENST00000255266.9:c.1473+29del	ENSP00000255266.5:n.1473+29del
ENST00000508173.5:n.1478del
ENST00000613228.1:c.1230+29del	ENSP00000478060.1:n.1230+29del
ENST00000617647.4:c.1230+29del	ENSP00000482774.1:n.1230+29del
NM_000440.2:c.1473+29del	NP_000431.2:n.1473+29del
XM_011537648.1:c.1473+29del	XP_011535950.1:n.1473+29del
XM_011537649.1:c.927+29del	XP_011535951.1:n.927+29del
XM_011537650.1:c.588+29del	XP_011535952.1:n.588+29del
XM_011537651.1:c.426+29del	XP_011535953.1:n.426+29del
XM_011537652.1:c.396+29del	XP_011535954.1:n.396+29del
XM_011537653.1:c.396+29del	XP_011535955.1:n.396+29del
XM_011537654.1:c.396+29del	XP_011535956.1:n.396+29del
XM_011537650.2:c.588+29del	XP_011535952.1:n.588+29del
XM_011537651.2:c.426+29del	XP_011535953.1:n.426+29del
XM_011537653.2:c.396+29del	XP_011535955.1:n.396+29del
XM_011537654.2:c.396+29del	XP_011535956.1:n.396+29del
XM_017009572.2:c.1230+29del	XP_016865061.1:n.1230+29del
NM_000440.3:c.1473+29del MANE Select	NP_000431.2:n.1473+29del