Canonical Allele Identifier: CA2063944337
Gene: OAS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.112919637G= , CM000674.2:g.112919637G= GRCh38
NC_000012.11:g.113357442G= , CM000674.1:g.113357442G= GRCh37
NC_000012.10:g.111841825G= NCBI36
NG_011530.1:g.17704G=
NG_011530.2:g.17704G=

Transcript Alleles

HGVS Amino-acid Change
NM_016816.4:c.*84G= MANE Select NP_058132.2:n.*84G=
ENST00000202917.10:c.*84G= MANE Select ENSP00000202917.5:n.*84G=
NM_001032409.1:c.1189G= NP_001027581.1:p.Gly397=
NM_001032409.2:c.1189G= NP_001027581.1:p.Gly397=
NM_001032409.3:c.1189G= NP_001027581.1:p.Gly397=
NM_001320151.1:c.1038+1937G= NP_001307080.1:n.1038+1937G=
NM_001320151.2:c.1038+1937G= NP_001307080.1:n.1038+1937G=
NM_016816.2:c.*84G= NP_058132.2:n.*84G=
NM_016816.3:c.*84G= NP_058132.2:n.*84G=
ENST00000202917.9:c.*84G= ENSP00000202917.5:n.*84G=
ENST00000445409.6:c.1189G= ENSP00000388001.2:p.Gly397=
ENST00000445409.7:c.1189G= ENSP00000388001.2:p.Gly397=
ENST00000452357.7:c.*1880G= ENSP00000415721.2:n.*1880G=
ENST00000540589.2:c.130+22G=
ENST00000540589.3:c.1167+22G= ENSP00000474083.2:n.1167+22G=
ENST00000549820.2:n.2162G=
ENST00000550883.2:c.*2862G= ENSP00000450286.2:n.*2862G=
ENST00000551241.5:c.1038+1937G= ENSP00000448790.1:n.1038+1937G=
ENST00000551241.6:c.1038+1937G= ENSP00000448790.1:n.1038+1937G=
ENST00000552526.1:c.44+205G= ENSP00000475139.1:n.44+205G=
ENST00000552526.2:c.1082+205G= ENSP00000475139.2:n.1082+205G=
ENST00000553152.2:c.*924G= ENSP00000449053.2:n.*924G=
ENST00000679413.1:n.3505G=
ENST00000679467.1:c.*84G= ENSP00000506593.1:n.*84G=
ENST00000679494.1:c.1133G= ENSP00000505090.1:p.Arg378=
ENST00000679767.1:c.*628G= ENSP00000505476.1:n.*628G=
ENST00000679971.1:c.715G= ENSP00000505786.1:p.Gly239=
ENST00000679987.1:c.*84G= ENSP00000504970.1:n.*84G=
ENST00000680189.1:c.*84G= ENSP00000505572.1:n.*84G=
ENST00000680455.1:c.*84G= ENSP00000505165.1:n.*84G=
ENST00000680522.1:c.*796G= ENSP00000506485.1:n.*796G=
ENST00000680659.1:c.*275G= ENSP00000504942.1:n.*275G=
ENST00000680919.1:c.*581G= ENSP00000506474.1:n.*581G=
ENST00000680934.1:c.*84G= ENSP00000505028.1:n.*84G=
ENST00000681228.1:c.*84G= ENSP00000505703.1:n.*84G=
ENST00000681436.1:n.7274G=
ENST00000681505.1:c.*628G= ENSP00000505794.1:n.*628G=
ENST00000681700.1:c.*84G= ENSP00000506580.1:n.*84G=
ENST00000681934.1:c.*62+22G= ENSP00000505482.1:n.*62+22G=
XM_006719434.1:c.*924G= XP_006719497.1:n.*924G=
XM_006719434.2:c.*924G= XP_006719497.1:n.*924G=
XM_011538413.1:c.1165G= XP_011536715.1:p.Gly389=
XM_011538413.2:c.1165G= XP_011536715.1:p.Gly389=
XM_011538414.1:c.1038+1937G= XP_011536716.1:n.1038+1937G=
XM_017019361.2:c.*84G= XP_016874850.1:n.*84G=
XM_017019362.1:c.*84G= XP_016874851.1:n.*84G=
XR_944557.1:n.1330G=