Canonical Allele Identifier: CA6799996

Gene: OAS1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.112919404G>A , CM000674.2:g.112919404G>A	GRCh38
NC_000012.11:g.113357209G>A , CM000674.1:g.113357209G>A	GRCh37
NC_000012.10:g.111841592G>A	NCBI36
NG_011530.1:g.17471G>A
NG_011530.2:g.17471G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000202917.10:c.1054G>A MANE Select	ENSP00000202917.5:p.Ala352Thr
ENST00000445409.7:c.1039-83G>A	ENSP00000388001.2:n.1039-83G>A
ENST00000452357.7:c.*1647G>A	ENSP00000415721.2:n.*1647G>A
ENST00000540589.3:c.1039-83G>A	ENSP00000474083.2:n.1039-83G>A
ENST00000549820.2:n.1929G>A
ENST00000550883.2:c.*2629G>A	ENSP00000450286.2:n.*2629G>A
ENST00000551241.6:c.1038+1704G>A	ENSP00000448790.1:n.1038+1704G>A
ENST00000552526.2:c.1054G>A	ENSP00000475139.2:p.Ala352Thr
ENST00000553152.2:c.*691G>A	ENSP00000449053.2:n.*691G>A
ENST00000679413.1:n.3272G>A
ENST00000679467.1:c.1069G>A	ENSP00000506593.1:p.Ala357Thr
ENST00000679494.1:c.900G>A	ENSP00000505090.1:p.Val300=
ENST00000679767.1:c.*395G>A	ENSP00000505476.1:n.*395G>A
ENST00000679971.1:c.565-83G>A	ENSP00000505786.1:n.565-83G>A
ENST00000679987.1:c.1075G>A	ENSP00000504970.1:p.Ala359Thr
ENST00000680189.1:c.1054G>A	ENSP00000505572.1:p.Ala352Thr
ENST00000680455.1:c.580G>A	ENSP00000505165.1:p.Ala194Thr
ENST00000680522.1:c.*563G>A	ENSP00000506485.1:n.*563G>A
ENST00000680659.1:c.*42G>A	ENSP00000504942.1:n.*42G>A
ENST00000680919.1:c.*348G>A	ENSP00000506474.1:n.*348G>A
ENST00000680934.1:c.885-83G>A	ENSP00000505028.1:n.885-83G>A
ENST00000681228.1:c.967G>A	ENSP00000505703.1:p.Ala323Thr
ENST00000681436.1:n.7041G>A
ENST00000681505.1:c.*395G>A	ENSP00000505794.1:n.*395G>A
ENST00000681700.1:c.1030G>A	ENSP00000506580.1:p.Ala344Thr
ENST00000681934.1:c.1054G>A	ENSP00000505482.1:p.Ala352Thr
ENST00000202917.9:c.1054G>A	ENSP00000202917.5:p.Ala352Thr
ENST00000445409.6:c.1039-83G>A	ENSP00000388001.2:n.1039-83G>A
ENST00000551241.5:c.1038+1704G>A	ENSP00000448790.1:n.1038+1704G>A
ENST00000552526.1:c.16G>A	ENSP00000475139.1:p.Ala6Thr
NM_001032409.1:c.1039-83G>A	NP_001027581.1:n.1039-83G>A
NM_016816.2:c.1054G>A	NP_058132.2:p.Ala352Thr
XM_006719434.1:c.*691G>A	XP_006719497.1:n.*691G>A
XM_011538413.1:c.1015-83G>A	XP_011536715.1:n.1015-83G>A
XM_011538414.1:c.1038+1704G>A	XP_011536716.1:n.1038+1704G>A
XR_944557.1:n.1097G>A
NM_001032409.2:c.1039-83G>A	NP_001027581.1:n.1039-83G>A
NM_001320151.1:c.1038+1704G>A	NP_001307080.1:n.1038+1704G>A
NM_016816.3:c.1054G>A	NP_058132.2:p.Ala352Thr
XM_006719434.2:c.*691G>A	XP_006719497.1:n.*691G>A
XM_011538413.2:c.1015-83G>A	XP_011536715.1:n.1015-83G>A
XM_017019361.2:c.1030G>A	XP_016874850.1:p.Ala344Thr
XM_017019362.1:c.565G>A	XP_016874851.1:p.Ala189Thr
NM_016816.4:c.1054G>A MANE Select	NP_058132.2:p.Ala352Thr
NM_001032409.3:c.1039-83G>A	NP_001027581.1:n.1039-83G>A
NM_001320151.2:c.1038+1704G>A	NP_001307080.1:n.1038+1704G>A