Canonical Allele Identifier: CA388867393

Gene: RPGRIP1

Linked Data

• MyVariant Identifiers: chr14:g.21792983T>A (hg19) ; chr14:g.21324824T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21324824T>A , CM000676.2:g.21324824T>A	GRCh38
NC_000014.8:g.21792983T>A , CM000676.1:g.21792983T>A	GRCh37
NC_000014.7:g.20862823T>A	NCBI36
NG_008933.1:g.41848T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400017.7:c.1969T>A MANE Select	ENSP00000382895.2:p.Ser657Thr
ENST00000382933.8:c.689-2799T>A	ENSP00000372391.4:n.689-2799T>A
ENST00000400017.6:c.1969T>A	ENSP00000382895.2:p.Ser657Thr
ENST00000553500.5:n.328+99T>A
ENST00000553927.1:n.901T>A
ENST00000554303.1:c.355T>A	ENSP00000450426.1:p.Ser119Thr
ENST00000555322.5:c.396T>A
ENST00000555489.5:c.213-51T>A	ENSP00000451044.1:n.213-51T>A
ENST00000555587.5:c.394T>A	ENSP00000451262.1:p.Ser132Thr
ENST00000556336.5:c.1682-2799T>A	ENSP00000450445.1:n.1682-2799T>A
ENST00000557771.5:c.1855T>A	ENSP00000451219.1:p.Ser619Thr
NM_020366.3:c.1969T>A	NP_065099.3:p.Ser657Thr
XM_005267879.2:c.895T>A	XP_005267936.1:p.Ser299Thr
XM_005267880.2:c.862T>A	XP_005267937.1:p.Ser288Thr
XM_005267881.2:c.343T>A	XP_005267938.1:p.Ser115Thr
XM_011536978.1:c.895T>A	XP_011535280.1:p.Ser299Thr
XM_011536979.1:c.796+99T>A	XP_011535281.1:n.796+99T>A
XM_011536980.1:c.796+99T>A	XP_011535282.1:n.796+99T>A
XM_011536981.1:c.895T>A	XP_011535283.1:p.Ser299Thr
XM_011536982.1:c.796+99T>A	XP_011535284.1:n.796+99T>A
XM_011536983.1:c.1936T>A	XP_011535285.1:p.Ser646Thr
XM_005267881.3:c.343T>A	XP_005267938.1:p.Ser115Thr
XM_017021473.1:c.895T>A	XP_016876962.1:p.Ser299Thr
XM_024449663.1:c.895T>A	XP_024305431.1:p.Ser299Thr
XM_024449664.1:c.895T>A	XP_024305432.1:p.Ser299Thr
XM_024449665.1:c.796+99T>A	XP_024305433.1:n.796+99T>A
XM_024449666.1:c.796+99T>A	XP_024305434.1:n.796+99T>A
NM_001377523.1:c.689-2799T>A	NP_001364452.1:n.689-2799T>A
NM_001377948.1:c.895T>A	NP_001364877.1:p.Ser299Thr
NM_001377949.1:c.796+99T>A	NP_001364878.1:n.796+99T>A
NM_001377950.1:c.689-2799T>A	NP_001364879.1:n.689-2799T>A
NM_001377951.1:c.191-2799T>A	NP_001364880.1:n.191-2799T>A
NM_020366.4:c.1969T>A MANE Select	NP_065099.3:p.Ser657Thr