Canonical Allele Identifier: CA1698611557
Gene: RP9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.33096459T= , CM000669.2:g.33096459T= GRCh38
NC_000007.13:g.33136071T= , CM000669.1:g.33136071T= GRCh37
NC_000007.12:g.33102596T= NCBI36
NG_012968.1:g.17932A=

Transcript Alleles

HGVS Amino-acid change
ENST00000474370.2:n.2440+34A=
ENST00000492391.2:n.1591+34A=
ENST00000682645.1:n.3538+34A=
ENST00000683432.1:c.*642+34A= ENSP00000508174.1:n.*642+34A=
ENST00000684207.1:c.*30A= ENSP00000506942.1:n.*30A=
ENST00000297157.8:c.467+34A= MANE Select ENSP00000297157.3:n.467+34A=
ENST00000297157.7:c.467+34A= ENSP00000297157.3:n.467+34A=
ENST00000448915.1:c.365+34A= ENSP00000411577.1:n.365+34A=
NM_203288.1:c.467+34A= NP_976033.1:n.467+34A=
XM_011515468.1:c.365+34A= XP_011513770.1:n.365+34A=
XM_011515468.3:c.365+34A= XP_011513770.1:n.365+34A=
NM_203288.2:c.467+34A= MANE Select NP_976033.1:n.467+34A=