Canonical Allele Identifier: CA2800816060
Gene: RPGRIP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.21312096_21312097del , CM000676.2:g.21312096_21312097del GRCh38
NC_000014.8:g.21780255_21780256del , CM000676.1:g.21780255_21780256del GRCh37
NC_000014.7:g.20850095_20850096del NCBI36
NG_008933.1:g.29120_29121del

Transcript Alleles

HGVS Amino-acid Change
ENST00000400017.7:c.1077+126_1077+127del MANE Select ENSP00000382895.2:n.1077+126_1077+127del
ENST00000400017.6:c.1077+126_1077+127del ENSP00000382895.2:n.1077+126_1077+127del
ENST00000556336.5:c.996+126_996+127del ENSP00000450445.1:n.996+126_996+127del
ENST00000557771.5:c.996+126_996+127del ENSP00000451219.1:n.996+126_996+127del
NM_020366.3:c.1077+126_1077+127del NP_065099.3:n.1077+126_1077+127del
XM_011536983.1:c.1044+126_1044+127del XP_011535285.1:n.1044+126_1044+127del
NM_020366.4:c.1077+126_1077+127del MANE Select NP_065099.3:n.1077+126_1077+127del