Canonical Allele Identifier: CA1698611599
Gene: RP9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.33096562G= , CM000669.2:g.33096562G= GRCh38
NC_000007.13:g.33136174G= , CM000669.1:g.33136174G= GRCh37
NC_000007.12:g.33102699G= NCBI36
NG_012968.1:g.17829C=

Transcript Alleles

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