Canonical Allele Identifier: CA1698611561
Gene: RP9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.33096473_33096476delinsTATC , CM000669.2:g.33096473_33096476delinsTATC GRCh38
NC_000007.13:g.33136085_33136088delinsTATC , CM000669.1:g.33136085_33136088delinsTATC GRCh37
NC_000007.12:g.33102610_33102613delinsTATC NCBI36
NG_012968.1:g.17915_17918delinsGATA

Transcript Alleles

HGVS Amino-acid change
ENST00000474370.2:n.2440+17_2440+20delinsGATA
ENST00000492391.2:n.1591+17_1591+20delinsGATA
ENST00000682645.1:n.3538+17_3538+20delinsGATA
ENST00000683432.1:c.*642+17_*642+20delinsGATA ENSP00000508174.1:n.*642+17_*642+20delins...
ENST00000684207.1:c.*13_*16delinsGATA ENSP00000506942.1:n.*13_*16delinsGATA
ENST00000297157.8:c.467+17_467+20delinsGATA MANE Select ENSP00000297157.3:n.467+17_467+20delinsGA...
ENST00000297157.7:c.467+17_467+20delinsGATA ENSP00000297157.3:n.467+17_467+20delinsGA...
ENST00000448915.1:c.365+17_365+20delinsGATA ENSP00000411577.1:n.365+17_365+20delinsGA...
NM_203288.1:c.467+17_467+20delinsGATA NP_976033.1:n.467+17_467+20delinsGATA
XM_011515468.1:c.365+17_365+20delinsGATA XP_011513770.1:n.365+17_365+20delinsGATA
XM_011515468.3:c.365+17_365+20delinsGATA XP_011513770.1:n.365+17_365+20delinsGATA
NM_203288.2:c.467+17_467+20delinsGATA MANE Select NP_976033.1:n.467+17_467+20delinsGATA