Canonical Allele Identifier: CA367181466

Gene: RP9

Linked Data

• MyVariant Identifiers: chr7:g.33136144T>A (hg19) ; chr7:g.33096532T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096532T>A , CM000669.2:g.33096532T>A	GRCh38
NC_000007.13:g.33136144T>A , CM000669.1:g.33136144T>A	GRCh37
NC_000007.12:g.33102669T>A	NCBI36
NG_012968.1:g.17859A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2401A>T
ENST00000492391.2:n.1552A>T
ENST00000682645.1:n.3499A>T
ENST00000683432.1:c.*603A>T	ENSP00000508174.1:n.*603A>T
ENST00000684207.1:c.428A>T	ENSP00000506942.1:p.Asp143Val
ENST00000297157.8:c.428A>T MANE Select	ENSP00000297157.3:p.Asp143Val
ENST00000297157.7:c.428A>T	ENSP00000297157.3:p.Asp143Val
ENST00000448915.1:c.326A>T	ENSP00000411577.1:p.Asp109Val
NM_203288.1:c.428A>T	NP_976033.1:p.Asp143Val
XM_011515468.1:c.326A>T	XP_011513770.1:p.Asp109Val
XM_011515468.3:c.326A>T	XP_011513770.1:p.Asp109Val
NM_203288.2:c.428A>T MANE Select	NP_976033.1:p.Asp143Val