Canonical Allele Identifier: CA2163227
Community Standard Title: NM_002601.4(PDE6D):c.182G>A (p.Arg61Gln)
Gene: PDE6D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.231738096C>T , CM000664.2:g.231738096C>T GRCh38
NC_000002.11:g.232602806C>T , CM000664.1:g.232602806C>T GRCh37
NC_000002.10:g.232311050C>T NCBI36
NG_034064.1:g.48232G>A

Transcript Alleles

HGVS Amino-acid Change
NM_002601.4:c.182G>A MANE Select NP_002592.1:p.Arg61Gln
ENST00000287600.9:c.182G>A MANE Select ENSP00000287600.4:p.Arg61Gln
NM_001291018.1:c.182G>A NP_001277947.1:p.Arg61Gln
NM_001291018.2:c.182G>A NP_001277947.1:p.Arg61Gln
NM_002601.3:c.182G>A NP_002592.1:p.Arg61Gln
ENST00000287600.8:c.182G>A ENSP00000287600.4:p.Arg61Gln
ENST00000409772.5:c.182G>A ENSP00000387108.1:p.Arg61Gln
ENST00000428104.2:c.125G>A ENSP00000399098.2:p.Arg42Gln
ENST00000486044.1:n.331G>A
XM_011511342.1:c.125G>A XP_011509644.1:p.Arg42Gln