Canonical Allele Identifier: CA388867184

Gene: RPGRIP1

Linked Data

• MyVariant Identifiers: chr14:g.21792907C>G (hg19) ; chr14:g.21324748C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21324748C>G , CM000676.2:g.21324748C>G	GRCh38
NC_000014.8:g.21792907C>G , CM000676.1:g.21792907C>G	GRCh37
NC_000014.7:g.20862747C>G	NCBI36
NG_008933.1:g.41772C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400017.7:c.1893C>G MANE Select	ENSP00000382895.2:p.His631Gln
ENST00000382933.8:c.688+2744C>G	ENSP00000372391.4:n.688+2744C>G
ENST00000400017.6:c.1893C>G	ENSP00000382895.2:p.His631Gln
ENST00000553500.5:n.328+23C>G
ENST00000553927.1:n.825C>G
ENST00000554303.1:c.279C>G	ENSP00000450426.1:p.His93Gln
ENST00000555322.5:c.320C>G
ENST00000555489.5:c.212+23C>G	ENSP00000451044.1:n.212+23C>G
ENST00000555587.5:c.318C>G	ENSP00000451262.1:p.His106Gln
ENST00000556336.5:c.1681+2744C>G	ENSP00000450445.1:n.1681+2744C>G
ENST00000557771.5:c.1779C>G	ENSP00000451219.1:p.His593Gln
NM_020366.3:c.1893C>G	NP_065099.3:p.His631Gln
XM_005267879.2:c.819C>G	XP_005267936.1:p.His273Gln
XM_005267880.2:c.786C>G	XP_005267937.1:p.His262Gln
XM_005267881.2:c.267C>G	XP_005267938.1:p.His89Gln
XM_011536978.1:c.819C>G	XP_011535280.1:p.His273Gln
XM_011536979.1:c.796+23C>G	XP_011535281.1:n.796+23C>G
XM_011536980.1:c.796+23C>G	XP_011535282.1:n.796+23C>G
XM_011536981.1:c.819C>G	XP_011535283.1:p.His273Gln
XM_011536982.1:c.796+23C>G	XP_011535284.1:n.796+23C>G
XM_011536983.1:c.1860C>G	XP_011535285.1:p.His620Gln
XM_005267881.3:c.267C>G	XP_005267938.1:p.His89Gln
XM_017021473.1:c.819C>G	XP_016876962.1:p.His273Gln
XM_024449663.1:c.819C>G	XP_024305431.1:p.His273Gln
XM_024449664.1:c.819C>G	XP_024305432.1:p.His273Gln
XM_024449665.1:c.796+23C>G	XP_024305433.1:n.796+23C>G
XM_024449666.1:c.796+23C>G	XP_024305434.1:n.796+23C>G
NM_001377523.1:c.688+2744C>G	NP_001364452.1:n.688+2744C>G
NM_001377948.1:c.819C>G	NP_001364877.1:p.His273Gln
NM_001377949.1:c.796+23C>G	NP_001364878.1:n.796+23C>G
NM_001377950.1:c.688+2744C>G	NP_001364879.1:n.688+2744C>G
NM_001377951.1:c.190+2744C>G	NP_001364880.1:n.190+2744C>G
NM_020366.4:c.1893C>G MANE Select	NP_065099.3:p.His631Gln