Canonical Allele Identifier: CA1698611613

Gene: RP9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096594T= , CM000669.2:g.33096594T=	GRCh38
NC_000007.13:g.33136206T= , CM000669.1:g.33136206T=	GRCh37
NC_000007.12:g.33102731T=	NCBI36
NG_012968.1:g.17797A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2379-40A=
ENST00000492391.2:n.1530-40A=
ENST00000682645.1:n.3477-40A=
ENST00000683432.1:c.*581-40A=	ENSP00000508174.1:n.*581-40A=
ENST00000684207.1:c.406-40A=	ENSP00000506942.1:n.406-40A=
ENST00000297157.8:c.406-40A= MANE Select	ENSP00000297157.3:n.406-40A=
ENST00000297157.7:c.406-40A=	ENSP00000297157.3:n.406-40A=
ENST00000448915.1:c.304-40A=	ENSP00000411577.1:n.304-40A=
NM_203288.1:c.406-40A=	NP_976033.1:n.406-40A=
XM_011515468.1:c.304-40A=	XP_011513770.1:n.304-40A=
XM_011515468.3:c.304-40A=	XP_011513770.1:n.304-40A=
NM_203288.2:c.406-40A= MANE Select	NP_976033.1:n.406-40A=