Canonical Allele Identifier: CA1698611597
Gene: RP9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.33096558A= , CM000669.2:g.33096558A= GRCh38
NC_000007.13:g.33136170A= , CM000669.1:g.33136170A= GRCh37
NC_000007.12:g.33102695A= NCBI36
NG_012968.1:g.17833T=

Transcript Alleles

HGVS Amino-acid change
ENST00000474370.2:n.2379-4T=
ENST00000492391.2:n.1530-4T=
ENST00000682645.1:n.3477-4T=
ENST00000683432.1:c.*581-4T= ENSP00000508174.1:n.*581-4T=
ENST00000684207.1:c.406-4T= ENSP00000506942.1:n.406-4T=
ENST00000297157.8:c.406-4T= MANE Select ENSP00000297157.3:n.406-4T=
ENST00000297157.7:c.406-4T= ENSP00000297157.3:n.406-4T=
ENST00000448915.1:c.304-4T= ENSP00000411577.1:n.304-4T=
NM_203288.1:c.406-4T= NP_976033.1:n.406-4T=
XM_011515468.1:c.304-4T= XP_011513770.1:n.304-4T=
XM_011515468.3:c.304-4T= XP_011513770.1:n.304-4T=
NM_203288.2:c.406-4T= MANE Select NP_976033.1:n.406-4T=