Canonical Allele Identifier: CA312415536

Gene: RIN2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.19974667C>T , CM000682.2:g.19974667C>T	GRCh38
NC_000020.10:g.19955311C>T , CM000682.1:g.19955311C>T	GRCh37
NC_000020.9:g.19903311C>T	NCBI36
NG_016310.1:g.90102C>T
NG_016310.2:g.90102C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255006.12:c.642C>T MANE Select	ENSP00000255006.7:p.Ser214=
ENST00000648440.1:c.642C>T	ENSP00000498085.1:p.Ser214=
ENST00000255006.10:c.789C>T	ENSP00000255006.6:p.Ser263=
ENST00000440354.2:c.463+13856C>T	ENSP00000391239.2:n.463+13856C>T
ENST00000484638.1:n.486C>T
NM_001242581.1:c.789C>T	NP_001229510.1:p.Ser263=
NM_018993.3:c.642C>T	NP_061866.1:p.Ser214=
XM_005260731.2:c.642C>T	XP_005260788.1:p.Ser214=
XM_005260732.2:c.507C>T	XP_005260789.1:p.Ser169=
XM_005260733.2:c.24C>T	XP_005260790.1:p.Ser8=
XM_006723574.2:c.642C>T	XP_006723637.1:p.Ser214=
XM_006723575.2:c.642C>T	XP_006723638.1:p.Ser214=
XM_006723577.2:c.642C>T	XP_006723640.1:p.Ser214=
XM_011529255.1:c.738C>T	XP_011527557.1:p.Ser246=
XM_011529256.1:c.798C>T	XP_011527558.1:p.Ser266=
XM_011529257.1:c.642C>T	XP_011527559.1:p.Ser214=
XM_011529258.1:c.642C>T	XP_011527560.1:p.Ser214=
XM_011529259.1:c.483C>T	XP_011527561.1:p.Ser161=
XM_011529260.1:c.642C>T	XP_011527562.1:p.Ser214=
XM_006723574.4:c.642C>T	XP_006723637.1:p.Ser214=
XM_006723575.4:c.642C>T	XP_006723638.1:p.Ser214=
XM_011529255.2:c.843C>T	XP_011527557.2:p.Ser281=
XM_011529257.2:c.642C>T	XP_011527559.1:p.Ser214=
XM_011529258.2:c.642C>T	XP_011527560.1:p.Ser214=
XM_011529259.2:c.483C>T	XP_011527561.1:p.Ser161=
XM_017027887.1:c.789C>T	XP_016883376.1:p.Ser263=
XM_017027888.1:c.789C>T	XP_016883377.1:p.Ser263=
XM_017027889.1:c.732C>T	XP_016883378.1:p.Ser244=
XM_017027890.1:c.642C>T	XP_016883379.1:p.Ser214=
XM_017027891.1:c.507C>T	XP_016883380.1:p.Ser169=
XM_017027892.1:c.483C>T	XP_016883381.1:p.Ser161=
XM_017027893.1:c.843C>T	XP_016883382.1:p.Ser281=
XM_024451911.1:c.642C>T	XP_024307679.1:p.Ser214=
XM_024451912.1:c.642C>T	XP_024307680.1:p.Ser214=
XM_024451913.1:c.642C>T	XP_024307681.1:p.Ser214=
NM_001242581.2:c.789C>T	NP_001229510.1:p.Ser263=
NM_001378238.1:c.24C>T	NP_001365167.1:p.Ser8=
NM_018993.4:c.642C>T MANE Select	NP_061866.1:p.Ser214=