Canonical Allele Identifier: CA1698611594

Gene: RP9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096549A= , CM000669.2:g.33096549A=	GRCh38
NC_000007.13:g.33136161A= , CM000669.1:g.33136161A=	GRCh37
NC_000007.12:g.33102686A=	NCBI36
NG_012968.1:g.17842T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2384T=
ENST00000492391.2:n.1535T=
ENST00000682645.1:n.3482T=
ENST00000683432.1:c.*586T=	ENSP00000508174.1:n.*586T=
ENST00000684207.1:c.411T=	ENSP00000506942.1:p.His137=
ENST00000297157.8:c.411T= MANE Select	ENSP00000297157.3:p.His137=
ENST00000297157.7:c.411T=	ENSP00000297157.3:p.His137=
ENST00000448915.1:c.309T=	ENSP00000411577.1:p.His103=
NM_203288.1:c.411T=	NP_976033.1:p.His137=
XM_011515468.1:c.309T=	XP_011513770.1:p.His103=
XM_011515468.3:c.309T=	XP_011513770.1:p.His103=
NM_203288.2:c.411T= MANE Select	NP_976033.1:p.His137=