Canonical Allele Identifier: CA2122460527

Gene: RPGRIP1

Linked Data

• dbSNP Id: rs1882900123

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21324915dup , CM000676.2:g.21324915dup	GRCh38
NC_000014.8:g.21793074dup , CM000676.1:g.21793074dup	GRCh37
NC_000014.7:g.20862914dup	NCBI36
NG_008933.1:g.41939dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400017.7:c.2060dup MANE Select	ENSP00000382895.2:p.Asp687GlufsTer16
ENST00000382933.8:c.689-2708dup	ENSP00000372391.4:n.689-2708dup
ENST00000400017.6:c.2060dup	ENSP00000382895.2:p.Asp687GlufsTer16
ENST00000553500.5:n.328+190dup
ENST00000553927.1:n.992dup
ENST00000555322.5:c.487dup
ENST00000555489.5:c.253dup	ENSP00000451044.1:n.253dup
ENST00000555587.5:c.485dup	ENSP00000451262.1:p.Asp162GlufsTer16
ENST00000556336.5:c.1682-2708dup	ENSP00000450445.1:n.1682-2708dup
ENST00000557771.5:c.1946dup	ENSP00000451219.1:p.Asp649GlufsTer16
NM_020366.3:c.2060dup	NP_065099.3:p.Asp687GlufsTer16
XM_005267879.2:c.986dup	XP_005267936.1:p.Asp329GlufsTer16
XM_005267880.2:c.953dup	XP_005267937.1:p.Asp318GlufsTer16
XM_005267881.2:c.434dup	XP_005267938.1:p.Asp145GlufsTer16
XM_011536978.1:c.986dup	XP_011535280.1:p.Asp329GlufsTer16
XM_011536979.1:c.797-27dup	XP_011535281.1:n.797-27dup
XM_011536980.1:c.796+190dup	XP_011535282.1:n.796+190dup
XM_011536981.1:c.986dup	XP_011535283.1:p.Asp329GlufsTer16
XM_011536982.1:c.796+190dup	XP_011535284.1:n.796+190dup
XM_011536983.1:c.2027dup	XP_011535285.1:p.Asp676GlufsTer16
XM_005267881.3:c.434dup	XP_005267938.1:p.Asp145GlufsTer16
XM_017021473.1:c.986dup	XP_016876962.1:p.Asp329GlufsTer16
XM_024449663.1:c.986dup	XP_024305431.1:p.Asp329GlufsTer16
XM_024449664.1:c.986dup	XP_024305432.1:p.Asp329GlufsTer16
XM_024449665.1:c.796+190dup	XP_024305433.1:n.796+190dup
XM_024449666.1:c.796+190dup	XP_024305434.1:n.796+190dup
NM_001377523.1:c.689-2708dup	NP_001364452.1:n.689-2708dup
NM_001377948.1:c.986dup	NP_001364877.1:p.Asp329GlufsTer16
NM_001377949.1:c.796+190dup	NP_001364878.1:n.796+190dup
NM_001377950.1:c.689-2708dup	NP_001364879.1:n.689-2708dup
NM_001377951.1:c.191-2708dup	NP_001364880.1:n.191-2708dup
NM_020366.4:c.2060dup MANE Select	NP_065099.3:p.Asp687GlufsTer16