Canonical Allele Identifier: CA1698611582

Gene: RP9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096523C= , CM000669.2:g.33096523C=	GRCh38
NC_000007.13:g.33136135C= , CM000669.1:g.33136135C=	GRCh37
NC_000007.12:g.33102660C=	NCBI36
NG_012968.1:g.17868G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2410G=
ENST00000492391.2:n.1561G=
ENST00000682645.1:n.3508G=
ENST00000683432.1:c.*612G=	ENSP00000508174.1:n.*612G=
ENST00000684207.1:c.437G=	ENSP00000506942.1:p.Arg146=
ENST00000297157.8:c.437G= MANE Select	ENSP00000297157.3:p.Arg146=
ENST00000297157.7:c.437G=	ENSP00000297157.3:p.Arg146=
ENST00000448915.1:c.335G=	ENSP00000411577.1:p.Arg112=
NM_203288.1:c.437G=	NP_976033.1:p.Arg146=
XM_011515468.1:c.335G=	XP_011513770.1:p.Arg112=
XM_011515468.3:c.335G=	XP_011513770.1:p.Arg112=
NM_203288.2:c.437G= MANE Select	NP_976033.1:p.Arg146=