Canonical Allele Identifier: CA2122460387
Gene: RPGRIP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.21324855C= , CM000676.2:g.21324855C= GRCh38
NC_000014.8:g.21793014C= , CM000676.1:g.21793014C= GRCh37
NC_000014.7:g.20862854C= NCBI36
NG_008933.1:g.41879C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000400017.7:c.2000C= MANE Select ENSP00000382895.2:p.Pro667=
ENST00000382933.8:c.689-2768C= ENSP00000372391.4:n.689-2768C=
ENST00000400017.6:c.2000C= ENSP00000382895.2:p.Pro667=
ENST00000553500.5:n.328+130C=
ENST00000553927.1:n.932C=
ENST00000554303.1:c.386C= ENSP00000450426.1:p.Pro129=
ENST00000555322.5:c.427C=
ENST00000555489.5:c.213-20C= ENSP00000451044.1:n.213-20C=
ENST00000555587.5:c.425C= ENSP00000451262.1:p.Pro142=
ENST00000556336.5:c.1682-2768C= ENSP00000450445.1:n.1682-2768C=
ENST00000557771.5:c.1886C= ENSP00000451219.1:p.Pro629=
NM_020366.3:c.2000C= NP_065099.3:p.Pro667=
XM_005267879.2:c.926C= XP_005267936.1:p.Pro309=
XM_005267880.2:c.893C= XP_005267937.1:p.Pro298=
XM_005267881.2:c.374C= XP_005267938.1:p.Pro125=
XM_011536978.1:c.926C= XP_011535280.1:p.Pro309=
XM_011536979.1:c.797-87C= XP_011535281.1:n.797-87C=
XM_011536980.1:c.796+130C= XP_011535282.1:n.796+130C=
XM_011536981.1:c.926C= XP_011535283.1:p.Pro309=
XM_011536982.1:c.796+130C= XP_011535284.1:n.796+130C=
XM_011536983.1:c.1967C= XP_011535285.1:p.Pro656=
XM_005267881.3:c.374C= XP_005267938.1:p.Pro125=
XM_017021473.1:c.926C= XP_016876962.1:p.Pro309=
XM_024449663.1:c.926C= XP_024305431.1:p.Pro309=
XM_024449664.1:c.926C= XP_024305432.1:p.Pro309=
XM_024449665.1:c.796+130C= XP_024305433.1:n.796+130C=
XM_024449666.1:c.796+130C= XP_024305434.1:n.796+130C=
NM_001377523.1:c.689-2768C= NP_001364452.1:n.689-2768C=
NM_001377948.1:c.926C= NP_001364877.1:p.Pro309=
NM_001377949.1:c.796+130C= NP_001364878.1:n.796+130C=
NM_001377950.1:c.689-2768C= NP_001364879.1:n.689-2768C=
NM_001377951.1:c.191-2768C= NP_001364880.1:n.191-2768C=
NM_020366.4:c.2000C= MANE Select NP_065099.3:p.Pro667=