Canonical Allele Identifier: CA388866966

Gene: RPGRIP1

Linked Data

• MyVariant Identifiers: chr14:g.21792856T>G (hg19) ; chr14:g.21324697T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21324697T>G , CM000676.2:g.21324697T>G	GRCh38
NC_000014.8:g.21792856T>G , CM000676.1:g.21792856T>G	GRCh37
NC_000014.7:g.20862696T>G	NCBI36
NG_008933.1:g.41721T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400017.7:c.1842T>G MANE Select	ENSP00000382895.2:p.Asp614Glu
ENST00000382933.8:c.688+2693T>G	ENSP00000372391.4:n.688+2693T>G
ENST00000400017.6:c.1842T>G	ENSP00000382895.2:p.Asp614Glu
ENST00000553500.5:n.300T>G
ENST00000553927.1:n.774T>G
ENST00000554303.1:c.228T>G	ENSP00000450426.1:p.Asp76Glu
ENST00000555322.5:c.297-28T>G
ENST00000555489.5:c.184T>G	ENSP00000451044.1:n.184T>G
ENST00000555587.5:c.267T>G	ENSP00000451262.1:p.Asp89Glu
ENST00000556336.5:c.1681+2693T>G	ENSP00000450445.1:n.1681+2693T>G
ENST00000557771.5:c.1728T>G	ENSP00000451219.1:p.Asp576Glu
NM_020366.3:c.1842T>G	NP_065099.3:p.Asp614Glu
XM_005267879.2:c.768T>G	XP_005267936.1:p.Asp256Glu
XM_005267880.2:c.735T>G	XP_005267937.1:p.Asp245Glu
XM_005267881.2:c.216T>G	XP_005267938.1:p.Asp72Glu
XM_011536978.1:c.768T>G	XP_011535280.1:p.Asp256Glu
XM_011536979.1:c.768T>G	XP_011535281.1:p.Asp256Glu
XM_011536980.1:c.768T>G	XP_011535282.1:p.Asp256Glu
XM_011536981.1:c.768T>G	XP_011535283.1:p.Asp256Glu
XM_011536982.1:c.768T>G	XP_011535284.1:p.Asp256Glu
XM_011536983.1:c.1809T>G	XP_011535285.1:p.Asp603Glu
XM_005267881.3:c.216T>G	XP_005267938.1:p.Asp72Glu
XM_017021473.1:c.768T>G	XP_016876962.1:p.Asp256Glu
XM_024449663.1:c.768T>G	XP_024305431.1:p.Asp256Glu
XM_024449664.1:c.768T>G	XP_024305432.1:p.Asp256Glu
XM_024449665.1:c.768T>G	XP_024305433.1:p.Asp256Glu
XM_024449666.1:c.768T>G	XP_024305434.1:p.Asp256Glu
NM_001377523.1:c.688+2693T>G	NP_001364452.1:n.688+2693T>G
NM_001377948.1:c.768T>G	NP_001364877.1:p.Asp256Glu
NM_001377949.1:c.768T>G	NP_001364878.1:p.Asp256Glu
NM_001377950.1:c.688+2693T>G	NP_001364879.1:n.688+2693T>G
NM_001377951.1:c.190+2693T>G	NP_001364880.1:n.190+2693T>G
NM_020366.4:c.1842T>G MANE Select	NP_065099.3:p.Asp614Glu