Canonical Allele Identifier: CA16608335

Gene: RIN2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.19960795A>G , CM000682.2:g.19960795A>G	GRCh38
NC_000020.10:g.19941439A>G , CM000682.1:g.19941439A>G	GRCh37
NC_000020.9:g.19889439A>G	NCBI36
NG_016310.1:g.76230A>G
NG_016310.2:g.76230A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255006.12:c.447A>G MANE Select	ENSP00000255006.7:p.Ile149Met
ENST00000648440.1:c.447A>G	ENSP00000498085.1:p.Ile149Met
ENST00000255006.10:c.594A>G	ENSP00000255006.6:p.Ile198Met
ENST00000440354.2:c.447A>G	ENSP00000391239.2:p.Ile149Met
ENST00000467569.5:n.690A>G
ENST00000484638.1:n.364A>G
NM_001242581.1:c.594A>G	NP_001229510.1:p.Ile198Met
NM_018993.3:c.447A>G	NP_061866.1:p.Ile149Met
XM_005260731.2:c.447A>G	XP_005260788.1:p.Ile149Met
XM_005260732.2:c.312A>G	XP_005260789.1:p.Ile104Met
XM_005260733.2:c.-99A>G	XP_005260790.1:n.-99A>G
XM_006723574.2:c.447A>G	XP_006723637.1:p.Ile149Met
XM_006723575.2:c.447A>G	XP_006723638.1:p.Ile149Met
XM_006723577.2:c.447A>G	XP_006723640.1:p.Ile149Met
XM_011529255.1:c.543A>G	XP_011527557.1:p.Ile181Met
XM_011529256.1:c.603A>G	XP_011527558.1:p.Ile201Met
XM_011529257.1:c.447A>G	XP_011527559.1:p.Ile149Met
XM_011529258.1:c.447A>G	XP_011527560.1:p.Ile149Met
XM_011529259.1:c.288A>G	XP_011527561.1:p.Ile96Met
XM_011529260.1:c.447A>G	XP_011527562.1:p.Ile149Met
XM_006723574.4:c.447A>G	XP_006723637.1:p.Ile149Met
XM_006723575.4:c.447A>G	XP_006723638.1:p.Ile149Met
XM_011529255.2:c.648A>G	XP_011527557.2:p.Ile216Met
XM_011529257.2:c.447A>G	XP_011527559.1:p.Ile149Met
XM_011529258.2:c.447A>G	XP_011527560.1:p.Ile149Met
XM_011529259.2:c.288A>G	XP_011527561.1:p.Ile96Met
XM_017027887.1:c.594A>G	XP_016883376.1:p.Ile198Met
XM_017027888.1:c.594A>G	XP_016883377.1:p.Ile198Met
XM_017027889.1:c.537A>G	XP_016883378.1:p.Ile179Met
XM_017027890.1:c.447A>G	XP_016883379.1:p.Ile149Met
XM_017027891.1:c.312A>G	XP_016883380.1:p.Ile104Met
XM_017027892.1:c.288A>G	XP_016883381.1:p.Ile96Met
XM_017027893.1:c.648A>G	XP_016883382.1:p.Ile216Met
XM_024451911.1:c.447A>G	XP_024307679.1:p.Ile149Met
XM_024451912.1:c.447A>G	XP_024307680.1:p.Ile149Met
XM_024451913.1:c.447A>G	XP_024307681.1:p.Ile149Met
NM_001242581.2:c.594A>G	NP_001229510.1:p.Ile198Met
NM_001378238.1:c.-99A>G	NP_001365167.1:n.-99A>G
NM_018993.4:c.447A>G MANE Select	NP_061866.1:p.Ile149Met