Canonical Allele Identifier: CA388867450

Gene: RPGRIP1

Linked Data

• MyVariant Identifiers: chr14:g.21792995T>G (hg19) ; chr14:g.21324836T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21324836T>G , CM000676.2:g.21324836T>G	GRCh38
NC_000014.8:g.21792995T>G , CM000676.1:g.21792995T>G	GRCh37
NC_000014.7:g.20862835T>G	NCBI36
NG_008933.1:g.41860T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400017.7:c.1981T>G MANE Select	ENSP00000382895.2:p.Phe661Val
ENST00000382933.8:c.689-2787T>G	ENSP00000372391.4:n.689-2787T>G
ENST00000400017.6:c.1981T>G	ENSP00000382895.2:p.Phe661Val
ENST00000553500.5:n.328+111T>G
ENST00000553927.1:n.913T>G
ENST00000554303.1:c.367T>G	ENSP00000450426.1:p.Phe123Val
ENST00000555322.5:c.408T>G
ENST00000555489.5:c.213-39T>G	ENSP00000451044.1:n.213-39T>G
ENST00000555587.5:c.406T>G	ENSP00000451262.1:p.Phe136Val
ENST00000556336.5:c.1682-2787T>G	ENSP00000450445.1:n.1682-2787T>G
ENST00000557771.5:c.1867T>G	ENSP00000451219.1:p.Phe623Val
NM_020366.3:c.1981T>G	NP_065099.3:p.Phe661Val
XM_005267879.2:c.907T>G	XP_005267936.1:p.Phe303Val
XM_005267880.2:c.874T>G	XP_005267937.1:p.Phe292Val
XM_005267881.2:c.355T>G	XP_005267938.1:p.Phe119Val
XM_011536978.1:c.907T>G	XP_011535280.1:p.Phe303Val
XM_011536979.1:c.797-106T>G	XP_011535281.1:n.797-106T>G
XM_011536980.1:c.796+111T>G	XP_011535282.1:n.796+111T>G
XM_011536981.1:c.907T>G	XP_011535283.1:p.Phe303Val
XM_011536982.1:c.796+111T>G	XP_011535284.1:n.796+111T>G
XM_011536983.1:c.1948T>G	XP_011535285.1:p.Phe650Val
XM_005267881.3:c.355T>G	XP_005267938.1:p.Phe119Val
XM_017021473.1:c.907T>G	XP_016876962.1:p.Phe303Val
XM_024449663.1:c.907T>G	XP_024305431.1:p.Phe303Val
XM_024449664.1:c.907T>G	XP_024305432.1:p.Phe303Val
XM_024449665.1:c.796+111T>G	XP_024305433.1:n.796+111T>G
XM_024449666.1:c.796+111T>G	XP_024305434.1:n.796+111T>G
NM_001377523.1:c.689-2787T>G	NP_001364452.1:n.689-2787T>G
NM_001377948.1:c.907T>G	NP_001364877.1:p.Phe303Val
NM_001377949.1:c.796+111T>G	NP_001364878.1:n.796+111T>G
NM_001377950.1:c.689-2787T>G	NP_001364879.1:n.689-2787T>G
NM_001377951.1:c.191-2787T>G	NP_001364880.1:n.191-2787T>G
NM_020366.4:c.1981T>G MANE Select	NP_065099.3:p.Phe661Val