Canonical Allele Identifier: CA1698611661

Gene: RP9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096720A= , CM000669.2:g.33096720A=	GRCh38
NC_000007.13:g.33136332A= , CM000669.1:g.33136332A=	GRCh37
NC_000007.12:g.33102857A=	NCBI36
NG_012968.1:g.17671T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2379-166T=
ENST00000492391.2:n.1530-166T=
ENST00000682645.1:n.3477-166T=
ENST00000683432.1:c.*581-166T=	ENSP00000508174.1:n.*581-166T=
ENST00000684207.1:c.406-166T=	ENSP00000506942.1:n.406-166T=
ENST00000297157.8:c.406-166T= MANE Select	ENSP00000297157.3:n.406-166T=
ENST00000297157.7:c.406-166T=	ENSP00000297157.3:n.406-166T=
ENST00000448915.1:c.304-166T=	ENSP00000411577.1:n.304-166T=
NM_203288.1:c.406-166T=	NP_976033.1:n.406-166T=
XM_011515468.1:c.304-166T=	XP_011513770.1:n.304-166T=
XM_011515468.3:c.304-166T=	XP_011513770.1:n.304-166T=
NM_203288.2:c.406-166T= MANE Select	NP_976033.1:n.406-166T=