Canonical Allele Identifier: CA8839068

Gene: PDE6G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81653225G>A , CM000679.2:g.81653225G>A	GRCh38
NC_000017.10:g.79620255G>A , CM000679.1:g.79620255G>A	GRCh37
NC_000017.9:g.77230660G>A	NCBI36
NG_009834.1:g.8353C>T
NG_009834.2:g.15194C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_002602.4:c.81C>T MANE Select	NP_002593.1:p.Pro27=
ENST00000331056.10:c.81C>T MANE Select	ENSP00000328412.5:p.Pro27=
NM_001365724.1:c.81C>T	NP_001352653.1:p.Pro27=
NM_001365725.1:c.81C>T	NP_001352654.1:p.Pro27=
NM_002602.3:c.81C>T	NP_002593.1:p.Pro27=
NR_026872.1:n.86-1540C>T
NR_026872.2:n.51-1540C>T
NR_158591.1:n.70-1540C>T
ENST00000331056.9:c.81C>T	ENSP00000328412.5:p.Pro27=
ENST00000571004.1:c.81C>T	ENSP00000461464.1:p.Pro27=
ENST00000571224.5:c.81C>T	ENSP00000458167.1:p.Pro27=
ENST00000573076.5:c.231C>T	ENSP00000458567.1:p.Pro77=
ENST00000574024.1:c.80-1540C>T	ENSP00000460962.1:n.80-1540C>T
ENST00000574777.1:n.47-1540C>T
XM_006721942.2:c.231C>T	XP_006722005.1:p.Pro77=
XM_006721942.3:c.231C>T	XP_006722005.1:p.Pro77=
XM_017024734.1:c.291C>T	XP_016880223.1:p.Pro97=
XM_017024736.1:c.81C>T	XP_016880225.1:p.Pro27=