Canonical Allele Identifier: CA388867639
Gene: RPGRIP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.21324882A>C , CM000676.2:g.21324882A>C GRCh38
NC_000014.8:g.21793041A>C , CM000676.1:g.21793041A>C GRCh37
NC_000014.7:g.20862881A>C NCBI36
NG_008933.1:g.41906A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000400017.7:c.2027A>C MANE Select ENSP00000382895.2:p.Tyr676Ser
ENST00000382933.8:c.689-2741A>C ENSP00000372391.4:n.689-2741A>C
ENST00000400017.6:c.2027A>C ENSP00000382895.2:p.Tyr676Ser
ENST00000553500.5:n.328+157A>C
ENST00000553927.1:n.959A>C
ENST00000554303.1:c.413A>C ENSP00000450426.1:p.Tyr138Ser
ENST00000555322.5:c.454A>C
ENST00000555489.5:c.220A>C ENSP00000451044.1:n.220A>C
ENST00000555587.5:c.452A>C ENSP00000451262.1:p.Tyr151Ser
ENST00000556336.5:c.1682-2741A>C ENSP00000450445.1:n.1682-2741A>C
ENST00000557771.5:c.1913A>C ENSP00000451219.1:p.Tyr638Ser
NM_020366.3:c.2027A>C NP_065099.3:p.Tyr676Ser
XM_005267879.2:c.953A>C XP_005267936.1:p.Tyr318Ser
XM_005267880.2:c.920A>C XP_005267937.1:p.Tyr307Ser
XM_005267881.2:c.401A>C XP_005267938.1:p.Tyr134Ser
XM_011536978.1:c.953A>C XP_011535280.1:p.Tyr318Ser
XM_011536979.1:c.797-60A>C XP_011535281.1:n.797-60A>C
XM_011536980.1:c.796+157A>C XP_011535282.1:n.796+157A>C
XM_011536981.1:c.953A>C XP_011535283.1:p.Tyr318Ser
XM_011536982.1:c.796+157A>C XP_011535284.1:n.796+157A>C
XM_011536983.1:c.1994A>C XP_011535285.1:p.Tyr665Ser
XM_005267881.3:c.401A>C XP_005267938.1:p.Tyr134Ser
XM_017021473.1:c.953A>C XP_016876962.1:p.Tyr318Ser
XM_024449663.1:c.953A>C XP_024305431.1:p.Tyr318Ser
XM_024449664.1:c.953A>C XP_024305432.1:p.Tyr318Ser
XM_024449665.1:c.796+157A>C XP_024305433.1:n.796+157A>C
XM_024449666.1:c.796+157A>C XP_024305434.1:n.796+157A>C
NM_001377523.1:c.689-2741A>C NP_001364452.1:n.689-2741A>C
NM_001377948.1:c.953A>C NP_001364877.1:p.Tyr318Ser
NM_001377949.1:c.796+157A>C NP_001364878.1:n.796+157A>C
NM_001377950.1:c.689-2741A>C NP_001364879.1:n.689-2741A>C
NM_001377951.1:c.191-2741A>C NP_001364880.1:n.191-2741A>C
NM_020366.4:c.2027A>C MANE Select NP_065099.3:p.Tyr676Ser