Canonical Allele Identifier: CA454342389

Gene: RP9

Linked Data

• MyVariant Identifiers: chr7:g.33136136G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096524G>T , CM000669.2:g.33096524G>T	GRCh38
NC_000007.13:g.33136136G>T , CM000669.1:g.33136136G>T	GRCh37
NC_000007.12:g.33102661G>T	NCBI36
NG_012968.1:g.17867C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2409C>A
ENST00000492391.2:n.1560C>A
ENST00000682645.1:n.3507C>A
ENST00000683432.1:c.*611C>A	ENSP00000508174.1:n.*611C>A
ENST00000684207.1:c.436C>A	ENSP00000506942.1:p.Arg146=
ENST00000297157.8:c.436C>A MANE Select	ENSP00000297157.3:p.Arg146=
ENST00000297157.7:c.436C>A	ENSP00000297157.3:p.Arg146=
ENST00000448915.1:c.334C>A	ENSP00000411577.1:p.Arg112=
NM_203288.1:c.436C>A	NP_976033.1:p.Arg146=
XM_011515468.1:c.334C>A	XP_011513770.1:p.Arg112=
XM_011515468.3:c.334C>A	XP_011513770.1:p.Arg112=
NM_203288.2:c.436C>A MANE Select	NP_976033.1:p.Arg146=