Canonical Allele Identifier: CA9779812

Gene: RIN2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.19960723C>T , CM000682.2:g.19960723C>T	GRCh38
NC_000020.10:g.19941367C>T , CM000682.1:g.19941367C>T	GRCh37
NC_000020.9:g.19889367C>T	NCBI36
NG_016310.1:g.76158C>T
NG_016310.2:g.76158C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255006.12:c.375C>T MANE Select	ENSP00000255006.7:p.Thr125=
ENST00000648440.1:c.375C>T	ENSP00000498085.1:p.Thr125=
ENST00000255006.10:c.522C>T	ENSP00000255006.6:p.Thr174=
ENST00000440354.2:c.375C>T	ENSP00000391239.2:p.Thr125=
ENST00000467569.5:n.618C>T
ENST00000484638.1:n.292C>T
NM_001242581.1:c.522C>T	NP_001229510.1:p.Thr174=
NM_018993.3:c.375C>T	NP_061866.1:p.Thr125=
XM_005260731.2:c.375C>T	XP_005260788.1:p.Thr125=
XM_005260732.2:c.240C>T	XP_005260789.1:p.Thr80=
XM_005260733.2:c.-171C>T	XP_005260790.1:n.-171C>T
XM_006723574.2:c.375C>T	XP_006723637.1:p.Thr125=
XM_006723575.2:c.375C>T	XP_006723638.1:p.Thr125=
XM_006723577.2:c.375C>T	XP_006723640.1:p.Thr125=
XM_011529255.1:c.471C>T	XP_011527557.1:p.Thr157=
XM_011529256.1:c.531C>T	XP_011527558.1:p.Thr177=
XM_011529257.1:c.375C>T	XP_011527559.1:p.Thr125=
XM_011529258.1:c.375C>T	XP_011527560.1:p.Thr125=
XM_011529259.1:c.216C>T	XP_011527561.1:p.Thr72=
XM_011529260.1:c.375C>T	XP_011527562.1:p.Thr125=
XM_006723574.4:c.375C>T	XP_006723637.1:p.Thr125=
XM_006723575.4:c.375C>T	XP_006723638.1:p.Thr125=
XM_011529255.2:c.576C>T	XP_011527557.2:p.Thr192=
XM_011529257.2:c.375C>T	XP_011527559.1:p.Thr125=
XM_011529258.2:c.375C>T	XP_011527560.1:p.Thr125=
XM_011529259.2:c.216C>T	XP_011527561.1:p.Thr72=
XM_017027887.1:c.522C>T	XP_016883376.1:p.Thr174=
XM_017027888.1:c.522C>T	XP_016883377.1:p.Thr174=
XM_017027889.1:c.465C>T	XP_016883378.1:p.Thr155=
XM_017027890.1:c.375C>T	XP_016883379.1:p.Thr125=
XM_017027891.1:c.240C>T	XP_016883380.1:p.Thr80=
XM_017027892.1:c.216C>T	XP_016883381.1:p.Thr72=
XM_017027893.1:c.576C>T	XP_016883382.1:p.Thr192=
XM_024451911.1:c.375C>T	XP_024307679.1:p.Thr125=
XM_024451912.1:c.375C>T	XP_024307680.1:p.Thr125=
XM_024451913.1:c.375C>T	XP_024307681.1:p.Thr125=
NM_001242581.2:c.522C>T	NP_001229510.1:p.Thr174=
NM_001378238.1:c.-171C>T	NP_001365167.1:n.-171C>T
NM_018993.4:c.375C>T MANE Select	NP_061866.1:p.Thr125=