Canonical Allele Identifier: CA388867535

Gene: RPGRIP1

Linked Data

• MyVariant Identifiers: chr14:g.21793016T>G (hg19) ; chr14:g.21324857T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21324857T>G , CM000676.2:g.21324857T>G	GRCh38
NC_000014.8:g.21793016T>G , CM000676.1:g.21793016T>G	GRCh37
NC_000014.7:g.20862856T>G	NCBI36
NG_008933.1:g.41881T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400017.7:c.2002T>G MANE Select	ENSP00000382895.2:p.Leu668Val
ENST00000382933.8:c.689-2766T>G	ENSP00000372391.4:n.689-2766T>G
ENST00000400017.6:c.2002T>G	ENSP00000382895.2:p.Leu668Val
ENST00000553500.5:n.328+132T>G
ENST00000553927.1:n.934T>G
ENST00000554303.1:c.388T>G	ENSP00000450426.1:p.Leu130Val
ENST00000555322.5:c.429T>G
ENST00000555489.5:c.213-18T>G	ENSP00000451044.1:n.213-18T>G
ENST00000555587.5:c.427T>G	ENSP00000451262.1:p.Leu143Val
ENST00000556336.5:c.1682-2766T>G	ENSP00000450445.1:n.1682-2766T>G
ENST00000557771.5:c.1888T>G	ENSP00000451219.1:p.Leu630Val
NM_020366.3:c.2002T>G	NP_065099.3:p.Leu668Val
XM_005267879.2:c.928T>G	XP_005267936.1:p.Leu310Val
XM_005267880.2:c.895T>G	XP_005267937.1:p.Leu299Val
XM_005267881.2:c.376T>G	XP_005267938.1:p.Leu126Val
XM_011536978.1:c.928T>G	XP_011535280.1:p.Leu310Val
XM_011536979.1:c.797-85T>G	XP_011535281.1:n.797-85T>G
XM_011536980.1:c.796+132T>G	XP_011535282.1:n.796+132T>G
XM_011536981.1:c.928T>G	XP_011535283.1:p.Leu310Val
XM_011536982.1:c.796+132T>G	XP_011535284.1:n.796+132T>G
XM_011536983.1:c.1969T>G	XP_011535285.1:p.Leu657Val
XM_005267881.3:c.376T>G	XP_005267938.1:p.Leu126Val
XM_017021473.1:c.928T>G	XP_016876962.1:p.Leu310Val
XM_024449663.1:c.928T>G	XP_024305431.1:p.Leu310Val
XM_024449664.1:c.928T>G	XP_024305432.1:p.Leu310Val
XM_024449665.1:c.796+132T>G	XP_024305433.1:n.796+132T>G
XM_024449666.1:c.796+132T>G	XP_024305434.1:n.796+132T>G
NM_001377523.1:c.689-2766T>G	NP_001364452.1:n.689-2766T>G
NM_001377948.1:c.928T>G	NP_001364877.1:p.Leu310Val
NM_001377949.1:c.796+132T>G	NP_001364878.1:n.796+132T>G
NM_001377950.1:c.689-2766T>G	NP_001364879.1:n.689-2766T>G
NM_001377951.1:c.191-2766T>G	NP_001364880.1:n.191-2766T>G
NM_020366.4:c.2002T>G MANE Select	NP_065099.3:p.Leu668Val