Canonical Allele Identifier: CA484986207

Gene: RPGRIP1

Linked Data

• MyVariant Identifiers: chr14:g.21792865T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21324706T>C , CM000676.2:g.21324706T>C	GRCh38
NC_000014.8:g.21792865T>C , CM000676.1:g.21792865T>C	GRCh37
NC_000014.7:g.20862705T>C	NCBI36
NG_008933.1:g.41730T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400017.7:c.1851T>C MANE Select	ENSP00000382895.2:p.Asp617=
ENST00000382933.8:c.688+2702T>C	ENSP00000372391.4:n.688+2702T>C
ENST00000400017.6:c.1851T>C	ENSP00000382895.2:p.Asp617=
ENST00000553500.5:n.309T>C
ENST00000553927.1:n.783T>C
ENST00000554303.1:c.237T>C	ENSP00000450426.1:p.Asp79=
ENST00000555322.5:c.297-19T>C
ENST00000555489.5:c.193T>C	ENSP00000451044.1:n.193T>C
ENST00000555587.5:c.276T>C	ENSP00000451262.1:p.Asp92=
ENST00000556336.5:c.1681+2702T>C	ENSP00000450445.1:n.1681+2702T>C
ENST00000557771.5:c.1737T>C	ENSP00000451219.1:p.Asp579=
NM_020366.3:c.1851T>C	NP_065099.3:p.Asp617=
XM_005267879.2:c.777T>C	XP_005267936.1:p.Asp259=
XM_005267880.2:c.744T>C	XP_005267937.1:p.Asp248=
XM_005267881.2:c.225T>C	XP_005267938.1:p.Asp75=
XM_011536978.1:c.777T>C	XP_011535280.1:p.Asp259=
XM_011536979.1:c.777T>C	XP_011535281.1:p.Asp259=
XM_011536980.1:c.777T>C	XP_011535282.1:p.Asp259=
XM_011536981.1:c.777T>C	XP_011535283.1:p.Asp259=
XM_011536982.1:c.777T>C	XP_011535284.1:p.Asp259=
XM_011536983.1:c.1818T>C	XP_011535285.1:p.Asp606=
XM_005267881.3:c.225T>C	XP_005267938.1:p.Asp75=
XM_017021473.1:c.777T>C	XP_016876962.1:p.Asp259=
XM_024449663.1:c.777T>C	XP_024305431.1:p.Asp259=
XM_024449664.1:c.777T>C	XP_024305432.1:p.Asp259=
XM_024449665.1:c.777T>C	XP_024305433.1:p.Asp259=
XM_024449666.1:c.777T>C	XP_024305434.1:p.Asp259=
NM_001377523.1:c.688+2702T>C	NP_001364452.1:n.688+2702T>C
NM_001377948.1:c.777T>C	NP_001364877.1:p.Asp259=
NM_001377949.1:c.777T>C	NP_001364878.1:p.Asp259=
NM_001377950.1:c.688+2702T>C	NP_001364879.1:n.688+2702T>C
NM_001377951.1:c.190+2702T>C	NP_001364880.1:n.190+2702T>C
NM_020366.4:c.1851T>C MANE Select	NP_065099.3:p.Asp617=