Canonical Allele Identifier: CA2368596050
Gene: RIPOR3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.50588503C= , CM000682.2:g.50588503C= GRCh38
NC_000020.10:g.49205040C= , CM000682.1:g.49205040C= GRCh37
NC_000020.9:g.48638447C= NCBI36
NG_034040.1:g.108028G=

Transcript Alleles

HGVS Amino-acid change
ENST00000327979.8:c.2662-611G= MANE Select ENSP00000332663.3:n.2662-611G=
ENST00000045083.6:c.2650-611G= ENSP00000045083.2:n.2650-611G=
ENST00000327979.6:c.2650-611G= ENSP00000332663.2:n.2650-611G=
ENST00000462842.1:n.328-611G=
NM_001290268.1:c.2662-611G= NP_001277197.1:n.2662-611G=
NM_080829.3:c.2650-611G= NP_543019.2:n.2650-611G=
NR_110890.1:n.3223-611G=
XM_005260294.3:c.2662-611G= XP_005260351.1:n.2662-611G=
XM_006723713.2:c.2647-611G= XP_006723776.1:n.2647-611G=
XM_011528578.1:c.2662-611G= XP_011526880.1:n.2662-611G=
XM_011528579.1:c.2650-611G= XP_011526881.1:n.2650-611G=
XM_011528580.1:c.2650-611G= XP_011526882.1:n.2650-611G=
XM_011528581.1:c.2650-611G= XP_011526883.1:n.2650-611G=
XM_011528582.1:c.1972-611G= XP_011526884.1:n.1972-611G=
XM_011528585.1:c.1651-611G= XP_011526887.1:n.1651-611G=
XM_006723713.4:c.2647-611G= XP_006723776.1:n.2647-611G=
XM_011528578.2:c.2662-611G= XP_011526880.1:n.2662-611G=
XM_011528579.2:c.2650-611G= XP_011526881.1:n.2650-611G=
XM_011528580.2:c.2650-611G= XP_011526882.1:n.2650-611G=
XM_011528581.2:c.2650-611G= XP_011526883.1:n.2650-611G=
XM_011528585.2:c.1651-611G= XP_011526887.1:n.1651-611G=
XM_017027681.1:c.1972-611G= XP_016883170.1:n.1972-611G=
XR_001754183.1:n.3513-611G=
NM_001290268.2:c.2662-611G= MANE Select NP_001277197.1:n.2662-611G=
NR_110890.2:n.3235-611G=
NM_080829.4:c.2650-611G= NP_543019.2:n.2650-611G=