Canonical Allele Identifier: CA454342372

Gene: RP9

Linked Data

• MyVariant Identifiers: chr7:g.33136122T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096510T>A , CM000669.2:g.33096510T>A	GRCh38
NC_000007.13:g.33136122T>A , CM000669.1:g.33136122T>A	GRCh37
NC_000007.12:g.33102647T>A	NCBI36
NG_012968.1:g.17881A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2423A>T
ENST00000492391.2:n.1574A>T
ENST00000682645.1:n.3521A>T
ENST00000683432.1:c.*625A>T	ENSP00000508174.1:n.*625A>T
ENST00000684207.1:c.450A>T	ENSP00000506942.1:p.Arg150=
ENST00000297157.8:c.450A>T MANE Select	ENSP00000297157.3:p.Arg150=
ENST00000297157.7:c.450A>T	ENSP00000297157.3:p.Arg150=
ENST00000448915.1:c.348A>T	ENSP00000411577.1:p.Arg116=
NM_203288.1:c.450A>T	NP_976033.1:p.Arg150=
XM_011515468.1:c.348A>T	XP_011513770.1:p.Arg116=
XM_011515468.3:c.348A>T	XP_011513770.1:p.Arg116=
NM_203288.2:c.450A>T MANE Select	NP_976033.1:p.Arg150=