Canonical Allele Identifier: CA386811227

Gene: OAS1

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000202917.10:c.*84G>T MANE Select	ENSP00000202917.5:n.*84G>T
ENST00000445409.7:c.1189G>T	ENSP00000388001.2:p.Gly397Ter
ENST00000452357.7:c.*1880G>T	ENSP00000415721.2:n.*1880G>T
ENST00000540589.3:c.1167+22G>T	ENSP00000474083.2:n.1167+22G>T
ENST00000549820.2:n.2162G>T
ENST00000550883.2:c.*2862G>T	ENSP00000450286.2:n.*2862G>T
ENST00000551241.6:c.1038+1937G>T	ENSP00000448790.1:n.1038+1937G>T
ENST00000552526.2:c.1082+205G>T	ENSP00000475139.2:n.1082+205G>T
ENST00000553152.2:c.*924G>T	ENSP00000449053.2:n.*924G>T
ENST00000679413.1:n.3505G>T
ENST00000679467.1:c.*84G>T	ENSP00000506593.1:n.*84G>T
ENST00000679494.1:c.1133G>T	ENSP00000505090.1:p.Arg378Met
ENST00000679767.1:c.*628G>T	ENSP00000505476.1:n.*628G>T
ENST00000679971.1:c.715G>T	ENSP00000505786.1:p.Gly239Ter
ENST00000679987.1:c.*84G>T	ENSP00000504970.1:n.*84G>T
ENST00000680189.1:c.*84G>T	ENSP00000505572.1:n.*84G>T
ENST00000680455.1:c.*84G>T	ENSP00000505165.1:n.*84G>T
ENST00000680522.1:c.*796G>T	ENSP00000506485.1:n.*796G>T
ENST00000680659.1:c.*275G>T	ENSP00000504942.1:n.*275G>T
ENST00000680919.1:c.*581G>T	ENSP00000506474.1:n.*581G>T
ENST00000680934.1:c.*84G>T	ENSP00000505028.1:n.*84G>T
ENST00000681228.1:c.*84G>T	ENSP00000505703.1:n.*84G>T
ENST00000681436.1:n.7274G>T
ENST00000681505.1:c.*628G>T	ENSP00000505794.1:n.*628G>T
ENST00000681700.1:c.*84G>T	ENSP00000506580.1:n.*84G>T
ENST00000681934.1:c.*62+22G>T	ENSP00000505482.1:n.*62+22G>T
ENST00000202917.9:c.*84G>T	ENSP00000202917.5:n.*84G>T
ENST00000445409.6:c.1189G>T	ENSP00000388001.2:p.Gly397Ter
ENST00000540589.2:c.130+22G>T
ENST00000551241.5:c.1038+1937G>T	ENSP00000448790.1:n.1038+1937G>T
ENST00000552526.1:c.44+205G>T	ENSP00000475139.1:n.44+205G>T
NM_001032409.1:c.1189G>T	NP_001027581.1:p.Gly397Ter
NM_016816.2:c.*84G>T	NP_058132.2:n.*84G>T
XM_006719434.1:c.*924G>T	XP_006719497.1:n.*924G>T
XM_011538413.1:c.1165G>T	XP_011536715.1:p.Gly389Ter
XM_011538414.1:c.1038+1937G>T	XP_011536716.1:n.1038+1937G>T
XR_944557.1:n.1330G>T
NM_001032409.2:c.1189G>T	NP_001027581.1:p.Gly397Ter
NM_001320151.1:c.1038+1937G>T	NP_001307080.1:n.1038+1937G>T
NM_016816.3:c.*84G>T	NP_058132.2:n.*84G>T
XM_006719434.2:c.*924G>T	XP_006719497.1:n.*924G>T
XM_011538413.2:c.1165G>T	XP_011536715.1:p.Gly389Ter
XM_017019361.2:c.*84G>T	XP_016874850.1:n.*84G>T
XM_017019362.1:c.*84G>T	XP_016874851.1:n.*84G>T
NM_016816.4:c.*84G>T MANE Select	NP_058132.2:n.*84G>T
NM_001032409.3:c.1189G>T	NP_001027581.1:p.Gly397Ter
NM_001320151.2:c.1038+1937G>T	NP_001307080.1:n.1038+1937G>T