Canonical Allele Identifier: CA510156867

Gene: RIN2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.19974709G>A , CM000682.2:g.19974709G>A	GRCh38
NC_000020.10:g.19955353G>A , CM000682.1:g.19955353G>A	GRCh37
NC_000020.9:g.19903353G>A	NCBI36
NG_016310.1:g.90144G>A
NG_016310.2:g.90144G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255006.12:c.684G>A MANE Select	ENSP00000255006.7:p.Arg228=
ENST00000648440.1:c.684G>A	ENSP00000498085.1:p.Arg228=
ENST00000255006.10:c.831G>A	ENSP00000255006.6:p.Arg277=
ENST00000440354.2:c.463+13898G>A	ENSP00000391239.2:n.463+13898G>A
ENST00000484638.1:n.528G>A
NM_001242581.1:c.831G>A	NP_001229510.1:p.Arg277=
NM_018993.3:c.684G>A	NP_061866.1:p.Arg228=
XM_005260731.2:c.684G>A	XP_005260788.1:p.Arg228=
XM_005260732.2:c.549G>A	XP_005260789.1:p.Arg183=
XM_005260733.2:c.66G>A	XP_005260790.1:p.Arg22=
XM_006723574.2:c.684G>A	XP_006723637.1:p.Arg228=
XM_006723575.2:c.684G>A	XP_006723638.1:p.Arg228=
XM_006723577.2:c.684G>A	XP_006723640.1:p.Arg228=
XM_011529255.1:c.780G>A	XP_011527557.1:p.Arg260=
XM_011529256.1:c.840G>A	XP_011527558.1:p.Arg280=
XM_011529257.1:c.684G>A	XP_011527559.1:p.Arg228=
XM_011529258.1:c.684G>A	XP_011527560.1:p.Arg228=
XM_011529259.1:c.525G>A	XP_011527561.1:p.Arg175=
XM_011529260.1:c.684G>A	XP_011527562.1:p.Arg228=
XM_006723574.4:c.684G>A	XP_006723637.1:p.Arg228=
XM_006723575.4:c.684G>A	XP_006723638.1:p.Arg228=
XM_011529255.2:c.885G>A	XP_011527557.2:p.Arg295=
XM_011529257.2:c.684G>A	XP_011527559.1:p.Arg228=
XM_011529258.2:c.684G>A	XP_011527560.1:p.Arg228=
XM_011529259.2:c.525G>A	XP_011527561.1:p.Arg175=
XM_017027887.1:c.831G>A	XP_016883376.1:p.Arg277=
XM_017027888.1:c.831G>A	XP_016883377.1:p.Arg277=
XM_017027889.1:c.774G>A	XP_016883378.1:p.Arg258=
XM_017027890.1:c.684G>A	XP_016883379.1:p.Arg228=
XM_017027891.1:c.549G>A	XP_016883380.1:p.Arg183=
XM_017027892.1:c.525G>A	XP_016883381.1:p.Arg175=
XM_017027893.1:c.885G>A	XP_016883382.1:p.Arg295=
XM_024451911.1:c.684G>A	XP_024307679.1:p.Arg228=
XM_024451912.1:c.684G>A	XP_024307680.1:p.Arg228=
XM_024451913.1:c.684G>A	XP_024307681.1:p.Arg228=
NM_001242581.2:c.831G>A	NP_001229510.1:p.Arg277=
NM_001378238.1:c.66G>A	NP_001365167.1:p.Arg22=
NM_018993.4:c.684G>A MANE Select	NP_061866.1:p.Arg228=