Canonical Allele Identifier: CA484986356

Gene: RPGRIP1

Linked Data

• MyVariant Identifiers: chr14:g.21793048C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21324889C>T , CM000676.2:g.21324889C>T	GRCh38
NC_000014.8:g.21793048C>T , CM000676.1:g.21793048C>T	GRCh37
NC_000014.7:g.20862888C>T	NCBI36
NG_008933.1:g.41913C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400017.7:c.2034C>T MANE Select	ENSP00000382895.2:p.Phe678=
ENST00000382933.8:c.689-2734C>T	ENSP00000372391.4:n.689-2734C>T
ENST00000400017.6:c.2034C>T	ENSP00000382895.2:p.Phe678=
ENST00000553500.5:n.328+164C>T
ENST00000553927.1:n.966C>T
ENST00000554303.1:c.420C>T	ENSP00000450426.1:p.Phe140=
ENST00000555322.5:c.461C>T
ENST00000555489.5:c.227C>T	ENSP00000451044.1:n.227C>T
ENST00000555587.5:c.459C>T	ENSP00000451262.1:p.Phe153=
ENST00000556336.5:c.1682-2734C>T	ENSP00000450445.1:n.1682-2734C>T
ENST00000557771.5:c.1920C>T	ENSP00000451219.1:p.Phe640=
NM_020366.3:c.2034C>T	NP_065099.3:p.Phe678=
XM_005267879.2:c.960C>T	XP_005267936.1:p.Phe320=
XM_005267880.2:c.927C>T	XP_005267937.1:p.Phe309=
XM_005267881.2:c.408C>T	XP_005267938.1:p.Phe136=
XM_011536978.1:c.960C>T	XP_011535280.1:p.Phe320=
XM_011536979.1:c.797-53C>T	XP_011535281.1:n.797-53C>T
XM_011536980.1:c.796+164C>T	XP_011535282.1:n.796+164C>T
XM_011536981.1:c.960C>T	XP_011535283.1:p.Phe320=
XM_011536982.1:c.796+164C>T	XP_011535284.1:n.796+164C>T
XM_011536983.1:c.2001C>T	XP_011535285.1:p.Phe667=
XM_005267881.3:c.408C>T	XP_005267938.1:p.Phe136=
XM_017021473.1:c.960C>T	XP_016876962.1:p.Phe320=
XM_024449663.1:c.960C>T	XP_024305431.1:p.Phe320=
XM_024449664.1:c.960C>T	XP_024305432.1:p.Phe320=
XM_024449665.1:c.796+164C>T	XP_024305433.1:n.796+164C>T
XM_024449666.1:c.796+164C>T	XP_024305434.1:n.796+164C>T
NM_001377523.1:c.689-2734C>T	NP_001364452.1:n.689-2734C>T
NM_001377948.1:c.960C>T	NP_001364877.1:p.Phe320=
NM_001377949.1:c.796+164C>T	NP_001364878.1:n.796+164C>T
NM_001377950.1:c.689-2734C>T	NP_001364879.1:n.689-2734C>T
NM_001377951.1:c.191-2734C>T	NP_001364880.1:n.191-2734C>T
NM_020366.4:c.2034C>T MANE Select	NP_065099.3:p.Phe678=