Canonical Allele Identifier: CA9779809

Gene: RIN2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.19960713A>G , CM000682.2:g.19960713A>G	GRCh38
NC_000020.10:g.19941357A>G , CM000682.1:g.19941357A>G	GRCh37
NC_000020.9:g.19889357A>G	NCBI36
NG_016310.1:g.76148A>G
NG_016310.2:g.76148A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255006.12:c.365A>G MANE Select	ENSP00000255006.7:p.His122Arg
ENST00000648440.1:c.365A>G	ENSP00000498085.1:p.His122Arg
ENST00000255006.10:c.512A>G	ENSP00000255006.6:p.His171Arg
ENST00000440354.2:c.365A>G	ENSP00000391239.2:p.His122Arg
ENST00000467569.5:n.608A>G
ENST00000484638.1:n.282A>G
NM_001242581.1:c.512A>G	NP_001229510.1:p.His171Arg
NM_018993.3:c.365A>G	NP_061866.1:p.His122Arg
XM_005260731.2:c.365A>G	XP_005260788.1:p.His122Arg
XM_005260732.2:c.230A>G	XP_005260789.1:p.His77Arg
XM_005260733.2:c.-181A>G	XP_005260790.1:n.-181A>G
XM_006723574.2:c.365A>G	XP_006723637.1:p.His122Arg
XM_006723575.2:c.365A>G	XP_006723638.1:p.His122Arg
XM_006723577.2:c.365A>G	XP_006723640.1:p.His122Arg
XM_011529255.1:c.461A>G	XP_011527557.1:p.His154Arg
XM_011529256.1:c.521A>G	XP_011527558.1:p.His174Arg
XM_011529257.1:c.365A>G	XP_011527559.1:p.His122Arg
XM_011529258.1:c.365A>G	XP_011527560.1:p.His122Arg
XM_011529259.1:c.206A>G	XP_011527561.1:p.His69Arg
XM_011529260.1:c.365A>G	XP_011527562.1:p.His122Arg
XM_006723574.4:c.365A>G	XP_006723637.1:p.His122Arg
XM_006723575.4:c.365A>G	XP_006723638.1:p.His122Arg
XM_011529255.2:c.566A>G	XP_011527557.2:p.His189Arg
XM_011529257.2:c.365A>G	XP_011527559.1:p.His122Arg
XM_011529258.2:c.365A>G	XP_011527560.1:p.His122Arg
XM_011529259.2:c.206A>G	XP_011527561.1:p.His69Arg
XM_017027887.1:c.512A>G	XP_016883376.1:p.His171Arg
XM_017027888.1:c.512A>G	XP_016883377.1:p.His171Arg
XM_017027889.1:c.455A>G	XP_016883378.1:p.His152Arg
XM_017027890.1:c.365A>G	XP_016883379.1:p.His122Arg
XM_017027891.1:c.230A>G	XP_016883380.1:p.His77Arg
XM_017027892.1:c.206A>G	XP_016883381.1:p.His69Arg
XM_017027893.1:c.566A>G	XP_016883382.1:p.His189Arg
XM_024451911.1:c.365A>G	XP_024307679.1:p.His122Arg
XM_024451912.1:c.365A>G	XP_024307680.1:p.His122Arg
XM_024451913.1:c.365A>G	XP_024307681.1:p.His122Arg
NM_001242581.2:c.512A>G	NP_001229510.1:p.His171Arg
NM_001378238.1:c.-181A>G	NP_001365167.1:n.-181A>G
NM_018993.4:c.365A>G MANE Select	NP_061866.1:p.His122Arg