Canonical Allele Identifier: CA2122452649
Gene: RPGRIP1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.21312068T= , CM000676.2:g.21312068T= GRCh38
NC_000014.8:g.21780227T= , CM000676.1:g.21780227T= GRCh37
NC_000014.7:g.20850067T= NCBI36
NG_008933.1:g.29092T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000400017.7:c.1077+98T= MANE Select ENSP00000382895.2:n.1077+98T=
ENST00000400017.6:c.1077+98T= ENSP00000382895.2:n.1077+98T=
ENST00000556336.5:c.996+98T= ENSP00000450445.1:n.996+98T=
ENST00000557771.5:c.996+98T= ENSP00000451219.1:n.996+98T=
NM_020366.3:c.1077+98T= NP_065099.3:n.1077+98T=
XM_011536983.1:c.1044+98T= XP_011535285.1:n.1044+98T=
NM_020366.4:c.1077+98T= MANE Select NP_065099.3:n.1077+98T=
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