Canonical Allele Identifier: CA1698611556
Gene: RP9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.33096458T= , CM000669.2:g.33096458T= GRCh38
NC_000007.13:g.33136070T= , CM000669.1:g.33136070T= GRCh37
NC_000007.12:g.33102595T= NCBI36
NG_012968.1:g.17933A=

Transcript Alleles

HGVS Amino-acid change
ENST00000474370.2:n.2440+35A=
ENST00000492391.2:n.1591+35A=
ENST00000682645.1:n.3538+35A=
ENST00000683432.1:c.*642+35A= ENSP00000508174.1:n.*642+35A=
ENST00000684207.1:c.*31A= ENSP00000506942.1:n.*31A=
ENST00000297157.8:c.467+35A= MANE Select ENSP00000297157.3:n.467+35A=
ENST00000297157.7:c.467+35A= ENSP00000297157.3:n.467+35A=
ENST00000448915.1:c.365+35A= ENSP00000411577.1:n.365+35A=
NM_203288.1:c.467+35A= NP_976033.1:n.467+35A=
XM_011515468.1:c.365+35A= XP_011513770.1:n.365+35A=
XM_011515468.3:c.365+35A= XP_011513770.1:n.365+35A=
NM_203288.2:c.467+35A= MANE Select NP_976033.1:n.467+35A=