Canonical Allele Identifier: CA388867816
Gene: RPGRIP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.21324925C>G , CM000676.2:g.21324925C>G GRCh38
NC_000014.8:g.21793084C>G , CM000676.1:g.21793084C>G GRCh37
NC_000014.7:g.20862924C>G NCBI36
NG_008933.1:g.41949C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000400017.7:c.2070C>G MANE Select ENSP00000382895.2:p.Phe690Leu
ENST00000382933.8:c.689-2698C>G ENSP00000372391.4:n.689-2698C>G
ENST00000400017.6:c.2070C>G ENSP00000382895.2:p.Phe690Leu
ENST00000553500.5:n.328+200C>G
ENST00000553927.1:n.1002C>G
ENST00000555322.5:c.497C>G
ENST00000555489.5:c.263C>G ENSP00000451044.1:n.263C>G
ENST00000555587.5:c.495C>G ENSP00000451262.1:p.Phe165Leu
ENST00000556336.5:c.1682-2698C>G ENSP00000450445.1:n.1682-2698C>G
ENST00000557771.5:c.1956C>G ENSP00000451219.1:p.Phe652Leu
NM_020366.3:c.2070C>G NP_065099.3:p.Phe690Leu
XM_005267879.2:c.996C>G XP_005267936.1:p.Phe332Leu
XM_005267880.2:c.963C>G XP_005267937.1:p.Phe321Leu
XM_005267881.2:c.444C>G XP_005267938.1:p.Phe148Leu
XM_011536978.1:c.996C>G XP_011535280.1:p.Phe332Leu
XM_011536979.1:c.797-17C>G XP_011535281.1:n.797-17C>G
XM_011536980.1:c.796+200C>G XP_011535282.1:n.796+200C>G
XM_011536981.1:c.996C>G XP_011535283.1:p.Phe332Leu
XM_011536982.1:c.796+200C>G XP_011535284.1:n.796+200C>G
XM_011536983.1:c.2037C>G XP_011535285.1:p.Phe679Leu
XM_005267881.3:c.444C>G XP_005267938.1:p.Phe148Leu
XM_017021473.1:c.996C>G XP_016876962.1:p.Phe332Leu
XM_024449663.1:c.996C>G XP_024305431.1:p.Phe332Leu
XM_024449664.1:c.996C>G XP_024305432.1:p.Phe332Leu
XM_024449665.1:c.796+200C>G XP_024305433.1:n.796+200C>G
XM_024449666.1:c.796+200C>G XP_024305434.1:n.796+200C>G
NM_001377523.1:c.689-2698C>G NP_001364452.1:n.689-2698C>G
NM_001377948.1:c.996C>G NP_001364877.1:p.Phe332Leu
NM_001377949.1:c.796+200C>G NP_001364878.1:n.796+200C>G
NM_001377950.1:c.689-2698C>G NP_001364879.1:n.689-2698C>G
NM_001377951.1:c.191-2698C>G NP_001364880.1:n.191-2698C>G
NM_020366.4:c.2070C>G MANE Select NP_065099.3:p.Phe690Leu