Canonical Allele Identifier: CA388866877

Gene: RPGRIP1

Linked Data

• MyVariant Identifiers: chr14:g.21792815T>G (hg19) ; chr14:g.21324656T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21324656T>G , CM000676.2:g.21324656T>G	GRCh38
NC_000014.8:g.21792815T>G , CM000676.1:g.21792815T>G	GRCh37
NC_000014.7:g.20862655T>G	NCBI36
NG_008933.1:g.41680T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400017.7:c.1801T>G MANE Select	ENSP00000382895.2:p.Ser601Ala
ENST00000382933.8:c.688+2652T>G	ENSP00000372391.4:n.688+2652T>G
ENST00000400017.6:c.1801T>G	ENSP00000382895.2:p.Ser601Ala
ENST00000553500.5:n.259T>G
ENST00000553927.1:n.733T>G
ENST00000554303.1:c.187T>G	ENSP00000450426.1:p.Ser63Ala
ENST00000555322.5:c.297-69T>G
ENST00000555489.5:c.143T>G	ENSP00000451044.1:p.Val48Gly
ENST00000555587.5:c.226T>G	ENSP00000451262.1:p.Ser76Ala
ENST00000556336.5:c.1681+2652T>G	ENSP00000450445.1:n.1681+2652T>G
ENST00000557771.5:c.1687T>G	ENSP00000451219.1:p.Ser563Ala
NM_020366.3:c.1801T>G	NP_065099.3:p.Ser601Ala
XM_005267879.2:c.727T>G	XP_005267936.1:p.Ser243Ala
XM_005267880.2:c.694T>G	XP_005267937.1:p.Ser232Ala
XM_005267881.2:c.175T>G	XP_005267938.1:p.Ser59Ala
XM_011536978.1:c.727T>G	XP_011535280.1:p.Ser243Ala
XM_011536979.1:c.727T>G	XP_011535281.1:p.Ser243Ala
XM_011536980.1:c.727T>G	XP_011535282.1:p.Ser243Ala
XM_011536981.1:c.727T>G	XP_011535283.1:p.Ser243Ala
XM_011536982.1:c.727T>G	XP_011535284.1:p.Ser243Ala
XM_011536983.1:c.1768T>G	XP_011535285.1:p.Ser590Ala
XM_005267881.3:c.175T>G	XP_005267938.1:p.Ser59Ala
XM_017021473.1:c.727T>G	XP_016876962.1:p.Ser243Ala
XM_024449663.1:c.727T>G	XP_024305431.1:p.Ser243Ala
XM_024449664.1:c.727T>G	XP_024305432.1:p.Ser243Ala
XM_024449665.1:c.727T>G	XP_024305433.1:p.Ser243Ala
XM_024449666.1:c.727T>G	XP_024305434.1:p.Ser243Ala
NM_001377523.1:c.688+2652T>G	NP_001364452.1:n.688+2652T>G
NM_001377948.1:c.727T>G	NP_001364877.1:p.Ser243Ala
NM_001377949.1:c.727T>G	NP_001364878.1:p.Ser243Ala
NM_001377950.1:c.688+2652T>G	NP_001364879.1:n.688+2652T>G
NM_001377951.1:c.190+2652T>G	NP_001364880.1:n.190+2652T>G
NM_020366.4:c.1801T>G MANE Select	NP_065099.3:p.Ser601Ala