Canonical Allele Identifier: CA2122460558
Gene: RPGRIP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.21324934C= , CM000676.2:g.21324934C= GRCh38
NC_000014.8:g.21793093C= , CM000676.1:g.21793093C= GRCh37
NC_000014.7:g.20862933C= NCBI36
NG_008933.1:g.41958C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000400017.7:c.2079C= MANE Select ENSP00000382895.2:p.Tyr693=
ENST00000382933.8:c.689-2689C= ENSP00000372391.4:n.689-2689C=
ENST00000400017.6:c.2079C= ENSP00000382895.2:p.Tyr693=
ENST00000553500.5:n.328+209C=
ENST00000553927.1:n.1011C=
ENST00000555322.5:c.506C=
ENST00000555489.5:c.272C= ENSP00000451044.1:n.272C=
ENST00000555587.5:c.504C= ENSP00000451262.1:p.Tyr168=
ENST00000556336.5:c.1682-2689C= ENSP00000450445.1:n.1682-2689C=
ENST00000557771.5:c.1965C= ENSP00000451219.1:p.Tyr655=
NM_020366.3:c.2079C= NP_065099.3:p.Tyr693=
XM_005267879.2:c.1005C= XP_005267936.1:p.Tyr335=
XM_005267880.2:c.972C= XP_005267937.1:p.Tyr324=
XM_005267881.2:c.453C= XP_005267938.1:p.Tyr151=
XM_011536978.1:c.1005C= XP_011535280.1:p.Tyr335=
XM_011536979.1:c.797-8C= XP_011535281.1:n.797-8C=
XM_011536980.1:c.796+209C= XP_011535282.1:n.796+209C=
XM_011536981.1:c.1005C= XP_011535283.1:p.Tyr335=
XM_011536982.1:c.796+209C= XP_011535284.1:n.796+209C=
XM_011536983.1:c.2046C= XP_011535285.1:p.Tyr682=
XM_005267881.3:c.453C= XP_005267938.1:p.Tyr151=
XM_017021473.1:c.1005C= XP_016876962.1:p.Tyr335=
XM_024449663.1:c.1005C= XP_024305431.1:p.Tyr335=
XM_024449664.1:c.1005C= XP_024305432.1:p.Tyr335=
XM_024449665.1:c.796+209C= XP_024305433.1:n.796+209C=
XM_024449666.1:c.796+209C= XP_024305434.1:n.796+209C=
NM_001377523.1:c.689-2689C= NP_001364452.1:n.689-2689C=
NM_001377948.1:c.1005C= NP_001364877.1:p.Tyr335=
NM_001377949.1:c.796+209C= NP_001364878.1:n.796+209C=
NM_001377950.1:c.689-2689C= NP_001364879.1:n.689-2689C=
NM_001377951.1:c.191-2689C= NP_001364880.1:n.191-2689C=
NM_020366.4:c.2079C= MANE Select NP_065099.3:p.Tyr693=