Canonical Allele Identifier: CA388866964
Gene: RPGRIP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.21324697T>A , CM000676.2:g.21324697T>A GRCh38
NC_000014.8:g.21792856T>A , CM000676.1:g.21792856T>A GRCh37
NC_000014.7:g.20862696T>A NCBI36
NG_008933.1:g.41721T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000400017.7:c.1842T>A MANE Select ENSP00000382895.2:p.Asp614Glu
ENST00000382933.8:c.688+2693T>A ENSP00000372391.4:n.688+2693T>A
ENST00000400017.6:c.1842T>A ENSP00000382895.2:p.Asp614Glu
ENST00000553500.5:n.300T>A
ENST00000553927.1:n.774T>A
ENST00000554303.1:c.228T>A ENSP00000450426.1:p.Asp76Glu
ENST00000555322.5:c.297-28T>A
ENST00000555489.5:c.184T>A ENSP00000451044.1:n.184T>A
ENST00000555587.5:c.267T>A ENSP00000451262.1:p.Asp89Glu
ENST00000556336.5:c.1681+2693T>A ENSP00000450445.1:n.1681+2693T>A
ENST00000557771.5:c.1728T>A ENSP00000451219.1:p.Asp576Glu
NM_020366.3:c.1842T>A NP_065099.3:p.Asp614Glu
XM_005267879.2:c.768T>A XP_005267936.1:p.Asp256Glu
XM_005267880.2:c.735T>A XP_005267937.1:p.Asp245Glu
XM_005267881.2:c.216T>A XP_005267938.1:p.Asp72Glu
XM_011536978.1:c.768T>A XP_011535280.1:p.Asp256Glu
XM_011536979.1:c.768T>A XP_011535281.1:p.Asp256Glu
XM_011536980.1:c.768T>A XP_011535282.1:p.Asp256Glu
XM_011536981.1:c.768T>A XP_011535283.1:p.Asp256Glu
XM_011536982.1:c.768T>A XP_011535284.1:p.Asp256Glu
XM_011536983.1:c.1809T>A XP_011535285.1:p.Asp603Glu
XM_005267881.3:c.216T>A XP_005267938.1:p.Asp72Glu
XM_017021473.1:c.768T>A XP_016876962.1:p.Asp256Glu
XM_024449663.1:c.768T>A XP_024305431.1:p.Asp256Glu
XM_024449664.1:c.768T>A XP_024305432.1:p.Asp256Glu
XM_024449665.1:c.768T>A XP_024305433.1:p.Asp256Glu
XM_024449666.1:c.768T>A XP_024305434.1:p.Asp256Glu
NM_001377523.1:c.688+2693T>A NP_001364452.1:n.688+2693T>A
NM_001377948.1:c.768T>A NP_001364877.1:p.Asp256Glu
NM_001377949.1:c.768T>A NP_001364878.1:p.Asp256Glu
NM_001377950.1:c.688+2693T>A NP_001364879.1:n.688+2693T>A
NM_001377951.1:c.190+2693T>A NP_001364880.1:n.190+2693T>A
NM_020366.4:c.1842T>A MANE Select NP_065099.3:p.Asp614Glu