Canonical Allele Identifier: CA156254167

Gene: RP9

Linked Data

• dbSNP Id: rs914296200
• MyVariant Identifiers: chr7:g.33136266_33136267insA (hg19) ; chr7:g.33096654_33096655insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096654_33096655insA , CM000669.2:g.33096654_33096655insA	GRCh38
NC_000007.13:g.33136266_33136267insA , CM000669.1:g.33136266_33136267insA	GRCh37
NC_000007.12:g.33102791_33102792insA	NCBI36
NG_012968.1:g.17736_17737insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2379-101_2379-100insT
ENST00000492391.2:n.1530-101_1530-100insT
ENST00000682645.1:n.3477-101_3477-100insT
ENST00000683432.1:c.*581-101_*581-100insT	ENSP00000508174.1:n.*581-101_*581-100insT
ENST00000684207.1:c.406-101_406-100insT	ENSP00000506942.1:n.406-101_406-100insT
ENST00000297157.8:c.406-101_406-100insT MANE Select	ENSP00000297157.3:n.406-101_406-100insT
ENST00000297157.7:c.406-101_406-100insT	ENSP00000297157.3:n.406-101_406-100insT
ENST00000448915.1:c.304-101_304-100insT	ENSP00000411577.1:n.304-101_304-100insT
NM_203288.1:c.406-101_406-100insT	NP_976033.1:n.406-101_406-100insT
XM_011515468.1:c.304-101_304-100insT	XP_011513770.1:n.304-101_304-100insT
XM_011515468.3:c.304-101_304-100insT	XP_011513770.1:n.304-101_304-100insT
NM_203288.2:c.406-101_406-100insT MANE Select	NP_976033.1:n.406-101_406-100insT