Canonical Allele Identifier: CA4974585
Gene: RIC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.5747420G>A , CM000671.2:g.5747420G>A GRCh38
NC_000009.11:g.5747420G>A , CM000671.1:g.5747420G>A GRCh37
NC_000009.10:g.5737420G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_020829.4:c.1367G>A MANE Select NP_065880.2:p.Arg456Gln
ENST00000414202.7:c.1367G>A MANE Select ENSP00000416696.2:p.Arg456Gln
NM_001135920.2:c.1367G>A NP_001129392.2:p.Arg456Gln
NM_001135920.3:c.1367G>A NP_001129392.2:p.Arg456Gln
NM_001135920.4:c.1367G>A NP_001129392.2:p.Arg456Gln
NM_001206557.1:c.1367G>A NP_001193486.1:p.Arg456Gln
NM_001206557.2:c.1367G>A NP_001193486.1:p.Arg456Gln
NM_020829.3:c.1367G>A NP_065880.2:p.Arg456Gln
ENST00000251879.10:c.1367G>A ENSP00000251879.6:p.Arg456Gln
ENST00000276898.3:n.2086G>A
ENST00000414202.6:c.1367G>A ENSP00000416696.2:p.Arg456Gln
ENST00000418622.7:c.1367G>A ENSP00000402240.4:p.Arg456Gln
ENST00000545641.5:c.1152G>A
XM_005251523.2:c.1364G>A XP_005251580.1:p.Arg455Gln
XM_005251523.3:c.1364G>A XP_005251580.1:p.Arg455Gln
XM_011517967.1:c.434G>A XP_011516269.1:p.Arg145Gln
XM_011517967.2:c.434G>A XP_011516269.1:p.Arg145Gln
XM_017014934.1:c.1022G>A XP_016870423.1:p.Arg341Gln
XM_017014935.1:c.1022G>A XP_016870424.1:p.Arg341Gln
XM_017014936.1:c.1022G>A XP_016870425.1:p.Arg341Gln
XR_428426.2:n.1647G>A
XR_428426.3:n.1647G>A