Canonical Allele Identifier: CA388867366

Gene: RPGRIP1

Linked Data

• MyVariant Identifiers: chr14:g.21792974T>C (hg19) ; chr14:g.21324815T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21324815T>C , CM000676.2:g.21324815T>C	GRCh38
NC_000014.8:g.21792974T>C , CM000676.1:g.21792974T>C	GRCh37
NC_000014.7:g.20862814T>C	NCBI36
NG_008933.1:g.41839T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400017.7:c.1960T>C MANE Select	ENSP00000382895.2:p.Cys654Arg
ENST00000382933.8:c.689-2808T>C	ENSP00000372391.4:n.689-2808T>C
ENST00000400017.6:c.1960T>C	ENSP00000382895.2:p.Cys654Arg
ENST00000553500.5:n.328+90T>C
ENST00000553927.1:n.892T>C
ENST00000554303.1:c.346T>C	ENSP00000450426.1:p.Cys116Arg
ENST00000555322.5:c.387T>C
ENST00000555489.5:c.213-60T>C	ENSP00000451044.1:n.213-60T>C
ENST00000555587.5:c.385T>C	ENSP00000451262.1:p.Cys129Arg
ENST00000556336.5:c.1682-2808T>C	ENSP00000450445.1:n.1682-2808T>C
ENST00000557771.5:c.1846T>C	ENSP00000451219.1:p.Cys616Arg
NM_020366.3:c.1960T>C	NP_065099.3:p.Cys654Arg
XM_005267879.2:c.886T>C	XP_005267936.1:p.Cys296Arg
XM_005267880.2:c.853T>C	XP_005267937.1:p.Cys285Arg
XM_005267881.2:c.334T>C	XP_005267938.1:p.Cys112Arg
XM_011536978.1:c.886T>C	XP_011535280.1:p.Cys296Arg
XM_011536979.1:c.796+90T>C	XP_011535281.1:n.796+90T>C
XM_011536980.1:c.796+90T>C	XP_011535282.1:n.796+90T>C
XM_011536981.1:c.886T>C	XP_011535283.1:p.Cys296Arg
XM_011536982.1:c.796+90T>C	XP_011535284.1:n.796+90T>C
XM_011536983.1:c.1927T>C	XP_011535285.1:p.Cys643Arg
XM_005267881.3:c.334T>C	XP_005267938.1:p.Cys112Arg
XM_017021473.1:c.886T>C	XP_016876962.1:p.Cys296Arg
XM_024449663.1:c.886T>C	XP_024305431.1:p.Cys296Arg
XM_024449664.1:c.886T>C	XP_024305432.1:p.Cys296Arg
XM_024449665.1:c.796+90T>C	XP_024305433.1:n.796+90T>C
XM_024449666.1:c.796+90T>C	XP_024305434.1:n.796+90T>C
NM_001377523.1:c.689-2808T>C	NP_001364452.1:n.689-2808T>C
NM_001377948.1:c.886T>C	NP_001364877.1:p.Cys296Arg
NM_001377949.1:c.796+90T>C	NP_001364878.1:n.796+90T>C
NM_001377950.1:c.689-2808T>C	NP_001364879.1:n.689-2808T>C
NM_001377951.1:c.191-2808T>C	NP_001364880.1:n.191-2808T>C
NM_020366.4:c.1960T>C MANE Select	NP_065099.3:p.Cys654Arg