Canonical Allele Identifier: CA1698611598
Gene: RP9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.33096560G= , CM000669.2:g.33096560G= GRCh38
NC_000007.13:g.33136172G= , CM000669.1:g.33136172G= GRCh37
NC_000007.12:g.33102697G= NCBI36
NG_012968.1:g.17831C=

Transcript Alleles

HGVS Amino-acid change
ENST00000474370.2:n.2379-6C=
ENST00000492391.2:n.1530-6C=
ENST00000682645.1:n.3477-6C=
ENST00000683432.1:c.*581-6C= ENSP00000508174.1:n.*581-6C=
ENST00000684207.1:c.406-6C= ENSP00000506942.1:n.406-6C=
ENST00000297157.8:c.406-6C= MANE Select ENSP00000297157.3:n.406-6C=
ENST00000297157.7:c.406-6C= ENSP00000297157.3:n.406-6C=
ENST00000448915.1:c.304-6C= ENSP00000411577.1:n.304-6C=
NM_203288.1:c.406-6C= NP_976033.1:n.406-6C=
XM_011515468.1:c.304-6C= XP_011513770.1:n.304-6C=
XM_011515468.3:c.304-6C= XP_011513770.1:n.304-6C=
NM_203288.2:c.406-6C= MANE Select NP_976033.1:n.406-6C=