Canonical Allele Identifier: CA388867699
Gene: RPGRIP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.21324897A>C , CM000676.2:g.21324897A>C GRCh38
NC_000014.8:g.21793056A>C , CM000676.1:g.21793056A>C GRCh37
NC_000014.7:g.20862896A>C NCBI36
NG_008933.1:g.41921A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000400017.7:c.2042A>C MANE Select ENSP00000382895.2:p.Gln681Pro
ENST00000382933.8:c.689-2726A>C ENSP00000372391.4:n.689-2726A>C
ENST00000400017.6:c.2042A>C ENSP00000382895.2:p.Gln681Pro
ENST00000553500.5:n.328+172A>C
ENST00000553927.1:n.974A>C
ENST00000554303.1:c.428A>C ENSP00000450426.1:p.Gln143Pro
ENST00000555322.5:c.469A>C
ENST00000555489.5:c.235A>C ENSP00000451044.1:n.235A>C
ENST00000555587.5:c.467A>C ENSP00000451262.1:p.Gln156Pro
ENST00000556336.5:c.1682-2726A>C ENSP00000450445.1:n.1682-2726A>C
ENST00000557771.5:c.1928A>C ENSP00000451219.1:p.Gln643Pro
NM_020366.3:c.2042A>C NP_065099.3:p.Gln681Pro
XM_005267879.2:c.968A>C XP_005267936.1:p.Gln323Pro
XM_005267880.2:c.935A>C XP_005267937.1:p.Gln312Pro
XM_005267881.2:c.416A>C XP_005267938.1:p.Gln139Pro
XM_011536978.1:c.968A>C XP_011535280.1:p.Gln323Pro
XM_011536979.1:c.797-45A>C XP_011535281.1:n.797-45A>C
XM_011536980.1:c.796+172A>C XP_011535282.1:n.796+172A>C
XM_011536981.1:c.968A>C XP_011535283.1:p.Gln323Pro
XM_011536982.1:c.796+172A>C XP_011535284.1:n.796+172A>C
XM_011536983.1:c.2009A>C XP_011535285.1:p.Gln670Pro
XM_005267881.3:c.416A>C XP_005267938.1:p.Gln139Pro
XM_017021473.1:c.968A>C XP_016876962.1:p.Gln323Pro
XM_024449663.1:c.968A>C XP_024305431.1:p.Gln323Pro
XM_024449664.1:c.968A>C XP_024305432.1:p.Gln323Pro
XM_024449665.1:c.796+172A>C XP_024305433.1:n.796+172A>C
XM_024449666.1:c.796+172A>C XP_024305434.1:n.796+172A>C
NM_001377523.1:c.689-2726A>C NP_001364452.1:n.689-2726A>C
NM_001377948.1:c.968A>C NP_001364877.1:p.Gln323Pro
NM_001377949.1:c.796+172A>C NP_001364878.1:n.796+172A>C
NM_001377950.1:c.689-2726A>C NP_001364879.1:n.689-2726A>C
NM_001377951.1:c.191-2726A>C NP_001364880.1:n.191-2726A>C
NM_020366.4:c.2042A>C MANE Select NP_065099.3:p.Gln681Pro