Canonical Allele Identifier: CA361695099

Gene: PDE6A

Linked Data

• MyVariant Identifiers: chr5:g.149274777T>G (hg19) ; chr5:g.149895214T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149895214T>G , CM000667.2:g.149895214T>G	GRCh38
NC_000005.9:g.149274777T>G , CM000667.1:g.149274777T>G	GRCh37
NC_000005.8:g.149254970T>G	NCBI36
NG_009102.1:g.54580A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255266.10:c.1697A>C MANE Select	ENSP00000255266.5:p.Asn566Thr
ENST00000255266.9:c.1697A>C	ENSP00000255266.5:p.Asn566Thr
ENST00000508173.5:n.1881A>C
ENST00000613228.1:c.1454A>C	ENSP00000478060.1:p.Asn485Thr
ENST00000617647.4:c.1454A>C	ENSP00000482774.1:p.Asn485Thr
NM_000440.2:c.1697A>C	NP_000431.2:p.Asn566Thr
XM_011537648.1:c.1697A>C	XP_011535950.1:p.Asn566Thr
XM_011537649.1:c.1151A>C	XP_011535951.1:p.Asn384Thr
XM_011537650.1:c.812A>C	XP_011535952.1:p.Asn271Thr
XM_011537651.1:c.650A>C	XP_011535953.1:p.Asn217Thr
XM_011537652.1:c.620A>C	XP_011535954.1:p.Asn207Thr
XM_011537653.1:c.620A>C	XP_011535955.1:p.Asn207Thr
XM_011537654.1:c.620A>C	XP_011535956.1:p.Asn207Thr
XM_011537650.2:c.812A>C	XP_011535952.1:p.Asn271Thr
XM_011537651.2:c.650A>C	XP_011535953.1:p.Asn217Thr
XM_011537653.2:c.620A>C	XP_011535955.1:p.Asn207Thr
XM_011537654.2:c.620A>C	XP_011535956.1:p.Asn207Thr
XM_017009572.2:c.1454A>C	XP_016865061.1:p.Asn485Thr
NM_000440.3:c.1697A>C MANE Select	NP_000431.2:p.Asn566Thr