Canonical Allele Identifier: CA2578864366
Gene: RP9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.33096557T>C , CM000669.2:g.33096557T>C GRCh38
NC_000007.13:g.33136169T>C , CM000669.1:g.33136169T>C GRCh37
NC_000007.12:g.33102694T>C NCBI36
NG_012968.1:g.17834A>G

Transcript Alleles

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