Canonical Allele Identifier: CA484986286

Gene: RPGRIP1

Linked Data

• MyVariant Identifiers: chr14:g.21792940A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21324781A>C , CM000676.2:g.21324781A>C	GRCh38
NC_000014.8:g.21792940A>C , CM000676.1:g.21792940A>C	GRCh37
NC_000014.7:g.20862780A>C	NCBI36
NG_008933.1:g.41805A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400017.7:c.1926A>C MANE Select	ENSP00000382895.2:p.Leu642=
ENST00000382933.8:c.688+2777A>C	ENSP00000372391.4:n.688+2777A>C
ENST00000400017.6:c.1926A>C	ENSP00000382895.2:p.Leu642=
ENST00000553500.5:n.328+56A>C
ENST00000553927.1:n.858A>C
ENST00000554303.1:c.312A>C	ENSP00000450426.1:p.Leu104=
ENST00000555322.5:c.353A>C
ENST00000555489.5:c.212+56A>C	ENSP00000451044.1:n.212+56A>C
ENST00000555587.5:c.351A>C	ENSP00000451262.1:p.Leu117=
ENST00000556336.5:c.1681+2777A>C	ENSP00000450445.1:n.1681+2777A>C
ENST00000557771.5:c.1812A>C	ENSP00000451219.1:p.Leu604=
NM_020366.3:c.1926A>C	NP_065099.3:p.Leu642=
XM_005267879.2:c.852A>C	XP_005267936.1:p.Leu284=
XM_005267880.2:c.819A>C	XP_005267937.1:p.Leu273=
XM_005267881.2:c.300A>C	XP_005267938.1:p.Leu100=
XM_011536978.1:c.852A>C	XP_011535280.1:p.Leu284=
XM_011536979.1:c.796+56A>C	XP_011535281.1:n.796+56A>C
XM_011536980.1:c.796+56A>C	XP_011535282.1:n.796+56A>C
XM_011536981.1:c.852A>C	XP_011535283.1:p.Leu284=
XM_011536982.1:c.796+56A>C	XP_011535284.1:n.796+56A>C
XM_011536983.1:c.1893A>C	XP_011535285.1:p.Leu631=
XM_005267881.3:c.300A>C	XP_005267938.1:p.Leu100=
XM_017021473.1:c.852A>C	XP_016876962.1:p.Leu284=
XM_024449663.1:c.852A>C	XP_024305431.1:p.Leu284=
XM_024449664.1:c.852A>C	XP_024305432.1:p.Leu284=
XM_024449665.1:c.796+56A>C	XP_024305433.1:n.796+56A>C
XM_024449666.1:c.796+56A>C	XP_024305434.1:n.796+56A>C
NM_001377523.1:c.688+2777A>C	NP_001364452.1:n.688+2777A>C
NM_001377948.1:c.852A>C	NP_001364877.1:p.Leu284=
NM_001377949.1:c.796+56A>C	NP_001364878.1:n.796+56A>C
NM_001377950.1:c.688+2777A>C	NP_001364879.1:n.688+2777A>C
NM_001377951.1:c.190+2777A>C	NP_001364880.1:n.190+2777A>C
NM_020366.4:c.1926A>C MANE Select	NP_065099.3:p.Leu642=