Canonical Allele Identifier: CA361693651

Gene: PDE6A

Linked Data

• MyVariant Identifiers: chr5:g.149265833C>A (hg19) ; chr5:g.149886270C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149886270C>A , CM000667.2:g.149886270C>A	GRCh38
NC_000005.9:g.149265833C>A , CM000667.1:g.149265833C>A	GRCh37
NC_000005.8:g.149246026C>A	NCBI36
NG_009102.1:g.63524G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255266.10:c.1833G>T MANE Select	ENSP00000255266.5:p.Gln611His
ENST00000255266.9:c.1833G>T	ENSP00000255266.5:p.Gln611His
ENST00000508173.5:n.2017G>T
ENST00000613228.1:c.1590G>T	ENSP00000478060.1:p.Gln530His
ENST00000617647.4:c.1590G>T	ENSP00000482774.1:p.Gln530His
NM_000440.2:c.1833G>T	NP_000431.2:p.Gln611His
XM_011537648.1:c.1833G>T	XP_011535950.1:p.Gln611His
XM_011537649.1:c.1287G>T	XP_011535951.1:p.Gln429His
XM_011537650.1:c.948G>T	XP_011535952.1:p.Gln316His
XM_011537651.1:c.786G>T	XP_011535953.1:p.Gln262His
XM_011537652.1:c.756G>T	XP_011535954.1:p.Gln252His
XM_011537653.1:c.756G>T	XP_011535955.1:p.Gln252His
XM_011537654.1:c.756G>T	XP_011535956.1:p.Gln252His
XM_011537650.2:c.948G>T	XP_011535952.1:p.Gln316His
XM_011537651.2:c.786G>T	XP_011535953.1:p.Gln262His
XM_011537653.2:c.756G>T	XP_011535955.1:p.Gln252His
XM_011537654.2:c.756G>T	XP_011535956.1:p.Gln252His
XM_017009572.2:c.1590G>T	XP_016865061.1:p.Gln530His
NM_000440.3:c.1833G>T MANE Select	NP_000431.2:p.Gln611His