Canonical Allele Identifier: CA367181363

Gene: RP9

Linked Data

• MyVariant Identifiers: chr7:g.33136129T>G (hg19) ; chr7:g.33096517T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096517T>G , CM000669.2:g.33096517T>G	GRCh38
NC_000007.13:g.33136129T>G , CM000669.1:g.33136129T>G	GRCh37
NC_000007.12:g.33102654T>G	NCBI36
NG_012968.1:g.17874A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2416A>C
ENST00000492391.2:n.1567A>C
ENST00000682645.1:n.3514A>C
ENST00000683432.1:c.*618A>C	ENSP00000508174.1:n.*618A>C
ENST00000684207.1:c.443A>C	ENSP00000506942.1:p.Asn148Thr
ENST00000297157.8:c.443A>C MANE Select	ENSP00000297157.3:p.Asn148Thr
ENST00000297157.7:c.443A>C	ENSP00000297157.3:p.Asn148Thr
ENST00000448915.1:c.341A>C	ENSP00000411577.1:p.Asn114Thr
NM_203288.1:c.443A>C	NP_976033.1:p.Asn148Thr
XM_011515468.1:c.341A>C	XP_011513770.1:p.Asn114Thr
XM_011515468.3:c.341A>C	XP_011513770.1:p.Asn114Thr
NM_203288.2:c.443A>C MANE Select	NP_976033.1:p.Asn148Thr