Canonical Allele Identifier: CA1698611587

Gene: RP9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096530T= , CM000669.2:g.33096530T=	GRCh38
NC_000007.13:g.33136142T= , CM000669.1:g.33136142T=	GRCh37
NC_000007.12:g.33102667T=	NCBI36
NG_012968.1:g.17861A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2403A=
ENST00000492391.2:n.1554A=
ENST00000682645.1:n.3501A=
ENST00000683432.1:c.*605A=	ENSP00000508174.1:n.*605A=
ENST00000684207.1:c.430A=	ENSP00000506942.1:p.Ile144=
ENST00000297157.8:c.430A= MANE Select	ENSP00000297157.3:p.Ile144=
ENST00000297157.7:c.430A=	ENSP00000297157.3:p.Ile144=
ENST00000448915.1:c.328A=	ENSP00000411577.1:p.Ile110=
NM_203288.1:c.430A=	NP_976033.1:p.Ile144=
XM_011515468.1:c.328A=	XP_011513770.1:p.Ile110=
XM_011515468.3:c.328A=	XP_011513770.1:p.Ile110=
NM_203288.2:c.430A= MANE Select	NP_976033.1:p.Ile144=