Canonical Allele Identifier: CA2580643935

Gene: RIPOR3

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.50588558G>T , CM000682.2:g.50588558G>T	GRCh38
NC_000020.10:g.49205095G>T , CM000682.1:g.49205095G>T	GRCh37
NC_000020.9:g.48638502G>T	NCBI36
NG_034040.1:g.107973C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000327979.8:c.2662-666C>A MANE Select	ENSP00000332663.3:n.2662-666C>A
ENST00000045083.6:c.2650-666C>A	ENSP00000045083.2:n.2650-666C>A
ENST00000327979.6:c.2650-666C>A	ENSP00000332663.2:n.2650-666C>A
ENST00000462842.1:n.328-666C>A
NM_001290268.1:c.2662-666C>A	NP_001277197.1:n.2662-666C>A
NM_080829.3:c.2650-666C>A	NP_543019.2:n.2650-666C>A
NR_110890.1:n.3223-666C>A
XM_005260294.3:c.2662-666C>A	XP_005260351.1:n.2662-666C>A
XM_006723713.2:c.2647-666C>A	XP_006723776.1:n.2647-666C>A
XM_011528578.1:c.2662-666C>A	XP_011526880.1:n.2662-666C>A
XM_011528579.1:c.2650-666C>A	XP_011526881.1:n.2650-666C>A
XM_011528580.1:c.2650-666C>A	XP_011526882.1:n.2650-666C>A
XM_011528581.1:c.2650-666C>A	XP_011526883.1:n.2650-666C>A
XM_011528582.1:c.1972-666C>A	XP_011526884.1:n.1972-666C>A
XM_011528585.1:c.1651-666C>A	XP_011526887.1:n.1651-666C>A
XM_006723713.4:c.2647-666C>A	XP_006723776.1:n.2647-666C>A
XM_011528578.2:c.2662-666C>A	XP_011526880.1:n.2662-666C>A
XM_011528579.2:c.2650-666C>A	XP_011526881.1:n.2650-666C>A
XM_011528580.2:c.2650-666C>A	XP_011526882.1:n.2650-666C>A
XM_011528581.2:c.2650-666C>A	XP_011526883.1:n.2650-666C>A
XM_011528585.2:c.1651-666C>A	XP_011526887.1:n.1651-666C>A
XM_017027681.1:c.1972-666C>A	XP_016883170.1:n.1972-666C>A
XR_001754183.1:n.3513-666C>A
NM_001290268.2:c.2662-666C>A MANE Select	NP_001277197.1:n.2662-666C>A
NR_110890.2:n.3235-666C>A
NM_080829.4:c.2650-666C>A	NP_543019.2:n.2650-666C>A