Canonical Allele Identifier: CA1698611537

Gene: RP9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096401T= , CM000669.2:g.33096401T=	GRCh38
NC_000007.13:g.33136013T= , CM000669.1:g.33136013T=	GRCh37
NC_000007.12:g.33102538T=	NCBI36
NG_012968.1:g.17990A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2440+92A=
ENST00000492391.2:n.1591+92A=
ENST00000682645.1:n.3538+92A=
ENST00000683432.1:c.*642+92A=	ENSP00000508174.1:n.*642+92A=
ENST00000684207.1:c.*88A=	ENSP00000506942.1:n.*88A=
ENST00000297157.8:c.467+92A= MANE Select	ENSP00000297157.3:n.467+92A=
ENST00000297157.7:c.467+92A=	ENSP00000297157.3:n.467+92A=
ENST00000448915.1:c.365+92A=	ENSP00000411577.1:n.365+92A=
NM_203288.1:c.467+92A=	NP_976033.1:n.467+92A=
XM_011515468.1:c.365+92A=	XP_011513770.1:n.365+92A=
XM_011515468.3:c.365+92A=	XP_011513770.1:n.365+92A=
NM_203288.2:c.467+92A= MANE Select	NP_976033.1:n.467+92A=