Canonical Allele Identifier: CA156254129

Gene: RP9

Linked Data

• dbSNP Id: rs35638614
• MyVariant Identifiers: chr7:g.33136205_33136206insT (hg19) ; chr7:g.33096593_33096594insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096594dup , CM000669.2:g.33096594dup	GRCh38
NC_000007.13:g.33136206dup , CM000669.1:g.33136206dup	GRCh37
NC_000007.12:g.33102731dup	NCBI36
NG_012968.1:g.17797dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2379-40dup
ENST00000492391.2:n.1530-40dup
ENST00000682645.1:n.3477-40dup
ENST00000683432.1:c.*581-40dup	ENSP00000508174.1:n.*581-40dup
ENST00000684207.1:c.406-40dup	ENSP00000506942.1:n.406-40dup
ENST00000297157.8:c.406-40dup MANE Select	ENSP00000297157.3:n.406-40dup
ENST00000297157.7:c.406-40dup	ENSP00000297157.3:n.406-40dup
ENST00000448915.1:c.304-40dup	ENSP00000411577.1:n.304-40dup
NM_203288.1:c.406-40dup	NP_976033.1:n.406-40dup
XM_011515468.1:c.304-40dup	XP_011513770.1:n.304-40dup
XM_011515468.3:c.304-40dup	XP_011513770.1:n.304-40dup
NM_203288.2:c.406-40dup MANE Select	NP_976033.1:n.406-40dup