Canonical Allele Identifier: CA388867201

Gene: RPGRIP1

Linked Data

• MyVariant Identifiers: chr14:g.21792911C>T (hg19) ; chr14:g.21324752C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21324752C>T , CM000676.2:g.21324752C>T	GRCh38
NC_000014.8:g.21792911C>T , CM000676.1:g.21792911C>T	GRCh37
NC_000014.7:g.20862751C>T	NCBI36
NG_008933.1:g.41776C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400017.7:c.1897C>T MANE Select	ENSP00000382895.2:p.His633Tyr
ENST00000382933.8:c.688+2748C>T	ENSP00000372391.4:n.688+2748C>T
ENST00000400017.6:c.1897C>T	ENSP00000382895.2:p.His633Tyr
ENST00000553500.5:n.328+27C>T
ENST00000553927.1:n.829C>T
ENST00000554303.1:c.283C>T	ENSP00000450426.1:p.His95Tyr
ENST00000555322.5:c.324C>T
ENST00000555489.5:c.212+27C>T	ENSP00000451044.1:n.212+27C>T
ENST00000555587.5:c.322C>T	ENSP00000451262.1:p.His108Tyr
ENST00000556336.5:c.1681+2748C>T	ENSP00000450445.1:n.1681+2748C>T
ENST00000557771.5:c.1783C>T	ENSP00000451219.1:p.His595Tyr
NM_020366.3:c.1897C>T	NP_065099.3:p.His633Tyr
XM_005267879.2:c.823C>T	XP_005267936.1:p.His275Tyr
XM_005267880.2:c.790C>T	XP_005267937.1:p.His264Tyr
XM_005267881.2:c.271C>T	XP_005267938.1:p.His91Tyr
XM_011536978.1:c.823C>T	XP_011535280.1:p.His275Tyr
XM_011536979.1:c.796+27C>T	XP_011535281.1:n.796+27C>T
XM_011536980.1:c.796+27C>T	XP_011535282.1:n.796+27C>T
XM_011536981.1:c.823C>T	XP_011535283.1:p.His275Tyr
XM_011536982.1:c.796+27C>T	XP_011535284.1:n.796+27C>T
XM_011536983.1:c.1864C>T	XP_011535285.1:p.His622Tyr
XM_005267881.3:c.271C>T	XP_005267938.1:p.His91Tyr
XM_017021473.1:c.823C>T	XP_016876962.1:p.His275Tyr
XM_024449663.1:c.823C>T	XP_024305431.1:p.His275Tyr
XM_024449664.1:c.823C>T	XP_024305432.1:p.His275Tyr
XM_024449665.1:c.796+27C>T	XP_024305433.1:n.796+27C>T
XM_024449666.1:c.796+27C>T	XP_024305434.1:n.796+27C>T
NM_001377523.1:c.688+2748C>T	NP_001364452.1:n.688+2748C>T
NM_001377948.1:c.823C>T	NP_001364877.1:p.His275Tyr
NM_001377949.1:c.796+27C>T	NP_001364878.1:n.796+27C>T
NM_001377950.1:c.688+2748C>T	NP_001364879.1:n.688+2748C>T
NM_001377951.1:c.190+2748C>T	NP_001364880.1:n.190+2748C>T
NM_020366.4:c.1897C>T MANE Select	NP_065099.3:p.His633Tyr