Canonical Allele Identifier: CA2063943862

Gene: OAS1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.112919432G= , CM000674.2:g.112919432G=	GRCh38
NC_000012.11:g.113357237G= , CM000674.1:g.113357237G=	GRCh37
NC_000012.10:g.111841620G=	NCBI36
NG_011530.1:g.17499G=
NG_011530.2:g.17499G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000202917.10:c.1082G= MANE Select	ENSP00000202917.5:p.Arg361=
ENST00000445409.7:c.1039-55G=	ENSP00000388001.2:n.1039-55G=
ENST00000452357.7:c.*1675G=	ENSP00000415721.2:n.*1675G=
ENST00000540589.3:c.1039-55G=	ENSP00000474083.2:n.1039-55G=
ENST00000549820.2:n.1957G=
ENST00000550883.2:c.*2657G=	ENSP00000450286.2:n.*2657G=
ENST00000551241.6:c.1038+1732G=	ENSP00000448790.1:n.1038+1732G=
ENST00000552526.2:c.1082G=	ENSP00000475139.2:p.Arg361=
ENST00000553152.2:c.*719G=	ENSP00000449053.2:n.*719G=
ENST00000679413.1:n.3300G=
ENST00000679467.1:c.1097G=	ENSP00000506593.1:p.Arg366=
ENST00000679494.1:c.928G=	ENSP00000505090.1:p.Gly310=
ENST00000679767.1:c.*423G=	ENSP00000505476.1:n.*423G=
ENST00000679971.1:c.565-55G=	ENSP00000505786.1:n.565-55G=
ENST00000679987.1:c.1103G=	ENSP00000504970.1:p.Arg368=
ENST00000680189.1:c.1082G=	ENSP00000505572.1:p.Arg361=
ENST00000680455.1:c.608G=	ENSP00000505165.1:p.Arg203=
ENST00000680522.1:c.*591G=	ENSP00000506485.1:n.*591G=
ENST00000680659.1:c.*70G=	ENSP00000504942.1:n.*70G=
ENST00000680919.1:c.*376G=	ENSP00000506474.1:n.*376G=
ENST00000680934.1:c.885-55G=	ENSP00000505028.1:n.885-55G=
ENST00000681228.1:c.995G=	ENSP00000505703.1:p.Arg332=
ENST00000681436.1:n.7069G=
ENST00000681505.1:c.*423G=	ENSP00000505794.1:n.*423G=
ENST00000681700.1:c.1058G=	ENSP00000506580.1:p.Arg353=
ENST00000681934.1:c.1082G=	ENSP00000505482.1:p.Arg361=
ENST00000202917.9:c.1082G=	ENSP00000202917.5:p.Arg361=
ENST00000445409.6:c.1039-55G=	ENSP00000388001.2:n.1039-55G=
ENST00000551241.5:c.1038+1732G=	ENSP00000448790.1:n.1038+1732G=
ENST00000552526.1:c.44G=	ENSP00000475139.1:p.Arg15=
NM_001032409.1:c.1039-55G=	NP_001027581.1:n.1039-55G=
NM_016816.2:c.1082G=	NP_058132.2:p.Arg361=
XM_006719434.1:c.*719G=	XP_006719497.1:n.*719G=
XM_011538413.1:c.1015-55G=	XP_011536715.1:n.1015-55G=
XM_011538414.1:c.1038+1732G=	XP_011536716.1:n.1038+1732G=
XR_944557.1:n.1125G=
NM_001032409.2:c.1039-55G=	NP_001027581.1:n.1039-55G=
NM_001320151.1:c.1038+1732G=	NP_001307080.1:n.1038+1732G=
NM_016816.3:c.1082G=	NP_058132.2:p.Arg361=
XM_006719434.2:c.*719G=	XP_006719497.1:n.*719G=
XM_011538413.2:c.1015-55G=	XP_011536715.1:n.1015-55G=
XM_017019361.2:c.1058G=	XP_016874850.1:p.Arg353=
XM_017019362.1:c.593G=	XP_016874851.1:p.Arg198=
NM_016816.4:c.1082G= MANE Select	NP_058132.2:p.Arg361=
NM_001032409.3:c.1039-55G=	NP_001027581.1:n.1039-55G=
NM_001320151.2:c.1038+1732G=	NP_001307080.1:n.1038+1732G=