Canonical Allele Identifier: CA454342406

Gene: RP9

Linked Data

• MyVariant Identifiers: chr7:g.33136152G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096540G>C , CM000669.2:g.33096540G>C	GRCh38
NC_000007.13:g.33136152G>C , CM000669.1:g.33136152G>C	GRCh37
NC_000007.12:g.33102677G>C	NCBI36
NG_012968.1:g.17851C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2393C>G
ENST00000492391.2:n.1544C>G
ENST00000682645.1:n.3491C>G
ENST00000683432.1:c.*595C>G	ENSP00000508174.1:n.*595C>G
ENST00000684207.1:c.420C>G	ENSP00000506942.1:p.Pro140=
ENST00000297157.8:c.420C>G MANE Select	ENSP00000297157.3:p.Pro140=
ENST00000297157.7:c.420C>G	ENSP00000297157.3:p.Pro140=
ENST00000448915.1:c.318C>G	ENSP00000411577.1:p.Pro106=
NM_203288.1:c.420C>G	NP_976033.1:p.Pro140=
XM_011515468.1:c.318C>G	XP_011513770.1:p.Pro106=
XM_011515468.3:c.318C>G	XP_011513770.1:p.Pro106=
NM_203288.2:c.420C>G MANE Select	NP_976033.1:p.Pro140=