Canonical Allele Identifier: CA1698611638

Gene: RP9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096656A= , CM000669.2:g.33096656A=	GRCh38
NC_000007.13:g.33136268A= , CM000669.1:g.33136268A=	GRCh37
NC_000007.12:g.33102793A=	NCBI36
NG_012968.1:g.17735T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2379-102T=
ENST00000492391.2:n.1530-102T=
ENST00000682645.1:n.3477-102T=
ENST00000683432.1:c.*581-102T=	ENSP00000508174.1:n.*581-102T=
ENST00000684207.1:c.406-102T=	ENSP00000506942.1:n.406-102T=
ENST00000297157.8:c.406-102T= MANE Select	ENSP00000297157.3:n.406-102T=
ENST00000297157.7:c.406-102T=	ENSP00000297157.3:n.406-102T=
ENST00000448915.1:c.304-102T=	ENSP00000411577.1:n.304-102T=
NM_203288.1:c.406-102T=	NP_976033.1:n.406-102T=
XM_011515468.1:c.304-102T=	XP_011513770.1:n.304-102T=
XM_011515468.3:c.304-102T=	XP_011513770.1:n.304-102T=
NM_203288.2:c.406-102T= MANE Select	NP_976033.1:n.406-102T=