Canonical Allele Identifier: CA9779962

Gene: RIN2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.19974928G>T , CM000682.2:g.19974928G>T	GRCh38
NC_000020.10:g.19955572G>T , CM000682.1:g.19955572G>T	GRCh37
NC_000020.9:g.19903572G>T	NCBI36
NG_016310.1:g.90363G>T
NG_016310.2:g.90363G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255006.12:c.903G>T MANE Select	ENSP00000255006.7:p.Thr301=
ENST00000648440.1:c.903G>T	ENSP00000498085.1:p.Thr301=
ENST00000255006.10:c.1050G>T	ENSP00000255006.6:p.Thr350=
ENST00000440354.2:c.463+14117G>T	ENSP00000391239.2:n.463+14117G>T
ENST00000484638.1:n.747G>T
NM_001242581.1:c.1050G>T	NP_001229510.1:p.Thr350=
NM_018993.3:c.903G>T	NP_061866.1:p.Thr301=
XM_005260731.2:c.903G>T	XP_005260788.1:p.Thr301=
XM_005260732.2:c.768G>T	XP_005260789.1:p.Thr256=
XM_005260733.2:c.285G>T	XP_005260790.1:p.Thr95=
XM_006723574.2:c.903G>T	XP_006723637.1:p.Thr301=
XM_006723575.2:c.903G>T	XP_006723638.1:p.Thr301=
XM_006723577.2:c.903G>T	XP_006723640.1:p.Thr301=
XM_011529255.1:c.999G>T	XP_011527557.1:p.Thr333=
XM_011529256.1:c.1059G>T	XP_011527558.1:p.Thr353=
XM_011529257.1:c.903G>T	XP_011527559.1:p.Thr301=
XM_011529258.1:c.903G>T	XP_011527560.1:p.Thr301=
XM_011529259.1:c.744G>T	XP_011527561.1:p.Thr248=
XM_011529260.1:c.903G>T	XP_011527562.1:p.Thr301=
XM_006723574.4:c.903G>T	XP_006723637.1:p.Thr301=
XM_006723575.4:c.903G>T	XP_006723638.1:p.Thr301=
XM_011529255.2:c.1104G>T	XP_011527557.2:p.Thr368=
XM_011529257.2:c.903G>T	XP_011527559.1:p.Thr301=
XM_011529258.2:c.903G>T	XP_011527560.1:p.Thr301=
XM_011529259.2:c.744G>T	XP_011527561.1:p.Thr248=
XM_017027887.1:c.1050G>T	XP_016883376.1:p.Thr350=
XM_017027888.1:c.1050G>T	XP_016883377.1:p.Thr350=
XM_017027889.1:c.993G>T	XP_016883378.1:p.Thr331=
XM_017027890.1:c.903G>T	XP_016883379.1:p.Thr301=
XM_017027891.1:c.768G>T	XP_016883380.1:p.Thr256=
XM_017027892.1:c.744G>T	XP_016883381.1:p.Thr248=
XM_017027893.1:c.1104G>T	XP_016883382.1:p.Thr368=
XM_024451911.1:c.903G>T	XP_024307679.1:p.Thr301=
XM_024451912.1:c.903G>T	XP_024307680.1:p.Thr301=
XM_024451913.1:c.903G>T	XP_024307681.1:p.Thr301=
NM_001242581.2:c.1050G>T	NP_001229510.1:p.Thr350=
NM_001378238.1:c.285G>T	NP_001365167.1:p.Thr95=
NM_018993.4:c.903G>T MANE Select	NP_061866.1:p.Thr301=