Canonical Allele Identifier: CA2122460133
Gene: RPGRIP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.21324739T= , CM000676.2:g.21324739T= GRCh38
NC_000014.8:g.21792898T= , CM000676.1:g.21792898T= GRCh37
NC_000014.7:g.20862738T= NCBI36
NG_008933.1:g.41763T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000400017.7:c.1884T= MANE Select ENSP00000382895.2:p.Phe628=
ENST00000382933.8:c.688+2735T= ENSP00000372391.4:n.688+2735T=
ENST00000400017.6:c.1884T= ENSP00000382895.2:p.Phe628=
ENST00000553500.5:n.328+14T=
ENST00000553927.1:n.816T=
ENST00000554303.1:c.270T= ENSP00000450426.1:p.Phe90=
ENST00000555322.5:c.311T=
ENST00000555489.5:c.212+14T= ENSP00000451044.1:n.212+14T=
ENST00000555587.5:c.309T= ENSP00000451262.1:p.Phe103=
ENST00000556336.5:c.1681+2735T= ENSP00000450445.1:n.1681+2735T=
ENST00000557771.5:c.1770T= ENSP00000451219.1:p.Phe590=
NM_020366.3:c.1884T= NP_065099.3:p.Phe628=
XM_005267879.2:c.810T= XP_005267936.1:p.Phe270=
XM_005267880.2:c.777T= XP_005267937.1:p.Phe259=
XM_005267881.2:c.258T= XP_005267938.1:p.Phe86=
XM_011536978.1:c.810T= XP_011535280.1:p.Phe270=
XM_011536979.1:c.796+14T= XP_011535281.1:n.796+14T=
XM_011536980.1:c.796+14T= XP_011535282.1:n.796+14T=
XM_011536981.1:c.810T= XP_011535283.1:p.Phe270=
XM_011536982.1:c.796+14T= XP_011535284.1:n.796+14T=
XM_011536983.1:c.1851T= XP_011535285.1:p.Phe617=
XM_005267881.3:c.258T= XP_005267938.1:p.Phe86=
XM_017021473.1:c.810T= XP_016876962.1:p.Phe270=
XM_024449663.1:c.810T= XP_024305431.1:p.Phe270=
XM_024449664.1:c.810T= XP_024305432.1:p.Phe270=
XM_024449665.1:c.796+14T= XP_024305433.1:n.796+14T=
XM_024449666.1:c.796+14T= XP_024305434.1:n.796+14T=
NM_001377523.1:c.688+2735T= NP_001364452.1:n.688+2735T=
NM_001377948.1:c.810T= NP_001364877.1:p.Phe270=
NM_001377949.1:c.796+14T= NP_001364878.1:n.796+14T=
NM_001377950.1:c.688+2735T= NP_001364879.1:n.688+2735T=
NM_001377951.1:c.190+2735T= NP_001364880.1:n.190+2735T=
NM_020366.4:c.1884T= MANE Select NP_065099.3:p.Phe628=