Canonical Allele Identifier: CA2122452666

Gene: RPGRIP1

Linked Data

• dbSNP Id: rs1594184481

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21312112T>G , CM000676.2:g.21312112T>G	GRCh38
NC_000014.8:g.21780271T>G , CM000676.1:g.21780271T>G	GRCh37
NC_000014.7:g.20850111T>G	NCBI36
NG_008933.1:g.29136T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400017.7:c.1077+142T>G MANE Select	ENSP00000382895.2:n.1077+142T>G
ENST00000400017.6:c.1077+142T>G	ENSP00000382895.2:n.1077+142T>G
ENST00000556336.5:c.996+142T>G	ENSP00000450445.1:n.996+142T>G
ENST00000557771.5:c.996+142T>G	ENSP00000451219.1:n.996+142T>G
NM_020366.3:c.1077+142T>G	NP_065099.3:n.1077+142T>G
XM_011536983.1:c.1044+142T>G	XP_011535285.1:n.1044+142T>G
NM_020366.4:c.1077+142T>G MANE Select	NP_065099.3:n.1077+142T>G