Canonical Allele Identifier: CA388867305

Gene: RPGRIP1

Linked Data

• MyVariant Identifiers: chr14:g.21792945A>C (hg19) ; chr14:g.21324786A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21324786A>C , CM000676.2:g.21324786A>C	GRCh38
NC_000014.8:g.21792945A>C , CM000676.1:g.21792945A>C	GRCh37
NC_000014.7:g.20862785A>C	NCBI36
NG_008933.1:g.41810A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400017.7:c.1931A>C MANE Select	ENSP00000382895.2:p.Gln644Pro
ENST00000382933.8:c.688+2782A>C	ENSP00000372391.4:n.688+2782A>C
ENST00000400017.6:c.1931A>C	ENSP00000382895.2:p.Gln644Pro
ENST00000553500.5:n.328+61A>C
ENST00000553927.1:n.863A>C
ENST00000554303.1:c.317A>C	ENSP00000450426.1:p.Gln106Pro
ENST00000555322.5:c.358A>C
ENST00000555489.5:c.212+61A>C	ENSP00000451044.1:n.212+61A>C
ENST00000555587.5:c.356A>C	ENSP00000451262.1:p.Gln119Pro
ENST00000556336.5:c.1681+2782A>C	ENSP00000450445.1:n.1681+2782A>C
ENST00000557771.5:c.1817A>C	ENSP00000451219.1:p.Gln606Pro
NM_020366.3:c.1931A>C	NP_065099.3:p.Gln644Pro
XM_005267879.2:c.857A>C	XP_005267936.1:p.Gln286Pro
XM_005267880.2:c.824A>C	XP_005267937.1:p.Gln275Pro
XM_005267881.2:c.305A>C	XP_005267938.1:p.Gln102Pro
XM_011536978.1:c.857A>C	XP_011535280.1:p.Gln286Pro
XM_011536979.1:c.796+61A>C	XP_011535281.1:n.796+61A>C
XM_011536980.1:c.796+61A>C	XP_011535282.1:n.796+61A>C
XM_011536981.1:c.857A>C	XP_011535283.1:p.Gln286Pro
XM_011536982.1:c.796+61A>C	XP_011535284.1:n.796+61A>C
XM_011536983.1:c.1898A>C	XP_011535285.1:p.Gln633Pro
XM_005267881.3:c.305A>C	XP_005267938.1:p.Gln102Pro
XM_017021473.1:c.857A>C	XP_016876962.1:p.Gln286Pro
XM_024449663.1:c.857A>C	XP_024305431.1:p.Gln286Pro
XM_024449664.1:c.857A>C	XP_024305432.1:p.Gln286Pro
XM_024449665.1:c.796+61A>C	XP_024305433.1:n.796+61A>C
XM_024449666.1:c.796+61A>C	XP_024305434.1:n.796+61A>C
NM_001377523.1:c.688+2782A>C	NP_001364452.1:n.688+2782A>C
NM_001377948.1:c.857A>C	NP_001364877.1:p.Gln286Pro
NM_001377949.1:c.796+61A>C	NP_001364878.1:n.796+61A>C
NM_001377950.1:c.688+2782A>C	NP_001364879.1:n.688+2782A>C
NM_001377951.1:c.190+2782A>C	NP_001364880.1:n.190+2782A>C
NM_020366.4:c.1931A>C MANE Select	NP_065099.3:p.Gln644Pro