Canonical Allele Identifier: CA2800816053
Gene: RPGRIP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.21312078del , CM000676.2:g.21312078del GRCh38
NC_000014.8:g.21780237del , CM000676.1:g.21780237del GRCh37
NC_000014.7:g.20850077del NCBI36
NG_008933.1:g.29102del

Transcript Alleles

HGVS Amino-acid Change
ENST00000400017.7:c.1077+108del MANE Select ENSP00000382895.2:n.1077+108del
ENST00000400017.6:c.1077+108del ENSP00000382895.2:n.1077+108del
ENST00000556336.5:c.996+108del ENSP00000450445.1:n.996+108del
ENST00000557771.5:c.996+108del ENSP00000451219.1:n.996+108del
NM_020366.3:c.1077+108del NP_065099.3:n.1077+108del
XM_011536983.1:c.1044+108del XP_011535285.1:n.1044+108del
NM_020366.4:c.1077+108del MANE Select NP_065099.3:n.1077+108del