Canonical Allele Identifier: CA123666

Gene: OAS1

Linked Data - Expert Curation

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.112911065G>A , CM000674.2:g.112911065G>A	GRCh38
NC_000012.11:g.113348870G>A , CM000674.1:g.113348870G>A	GRCh37
NC_000012.10:g.111833253G>A	NCBI36
NG_011530.1:g.9132G>A
NG_011530.2:g.9132G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000202917.10:c.484G>A MANE Select	ENSP00000202917.5:p.Gly162Ser
ENST00000445409.7:c.484G>A	ENSP00000388001.2:p.Gly162Ser
ENST00000452357.7:c.484G>A	ENSP00000415721.2:p.Gly162Ser
ENST00000540589.3:c.484G>A	ENSP00000474083.2:p.Gly162Ser
ENST00000549820.2:n.551G>A
ENST00000550689.2:c.470-33G>A	ENSP00000448348.2:n.470-33G>A
ENST00000550883.2:c.484G>A	ENSP00000450286.2:p.Gly162Ser
ENST00000551241.6:c.484G>A	ENSP00000448790.1:p.Gly162Ser
ENST00000552526.2:c.484G>A	ENSP00000475139.2:p.Gly162Ser
ENST00000553152.2:c.484G>A	ENSP00000449053.2:p.Gly162Ser
ENST00000675868.2:c.470-33G>A	ENSP00000502804.1:n.470-33G>A
ENST00000679467.1:c.499G>A	ENSP00000506593.1:p.Gly167Ser
ENST00000679494.1:c.484G>A	ENSP00000505090.1:p.Gly162Ser
ENST00000679767.1:c.469+2241G>A	ENSP00000505476.1:n.469+2241G>A
ENST00000679841.1:c.470-33G>A	ENSP00000505725.1:n.470-33G>A
ENST00000679971.1:c.180+3846G>A	ENSP00000505786.1:n.180+3846G>A
ENST00000679987.1:c.484G>A	ENSP00000504970.1:p.Gly162Ser
ENST00000680189.1:c.484G>A	ENSP00000505572.1:p.Gly162Ser
ENST00000680455.1:c.180+3846G>A	ENSP00000505165.1:n.180+3846G>A
ENST00000680522.1:c.479G>A	ENSP00000506485.1:p.Arg160Gln
ENST00000680659.1:c.484G>A	ENSP00000504942.1:p.Gly162Ser
ENST00000680919.1:c.484G>A	ENSP00000506474.1:p.Gly162Ser
ENST00000680934.1:c.484G>A	ENSP00000505028.1:p.Gly162Ser
ENST00000681228.1:c.397G>A	ENSP00000505703.1:p.Gly133Ser
ENST00000681436.1:n.390G>A
ENST00000681466.1:n.256G>A
ENST00000681505.1:c.470-33G>A	ENSP00000505794.1:n.470-33G>A
ENST00000681700.1:c.470-33G>A	ENSP00000506580.1:n.470-33G>A
ENST00000681831.1:n.1878G>A
ENST00000681934.1:c.484G>A	ENSP00000505482.1:p.Gly162Ser
ENST00000202917.9:c.484G>A	ENSP00000202917.5:p.Gly162Ser
ENST00000445409.6:c.484G>A	ENSP00000388001.2:p.Gly162Ser
ENST00000452357.6:c.484G>A	ENSP00000415721.2:p.Gly162Ser
ENST00000549820.1:n.537-33G>A
ENST00000550689.1:c.472G>A	ENSP00000448348.1:p.Gly158Ser
ENST00000550883.1:c.180+3846G>A	ENSP00000450286.1:n.180+3846G>A
ENST00000551241.5:c.484G>A	ENSP00000448790.1:p.Gly162Ser
NM_001032409.1:c.484G>A	NP_001027581.1:p.Gly162Ser
NM_002534.2:c.484G>A	NP_002525.2:p.Gly162Ser
NM_016816.2:c.484G>A	NP_058132.2:p.Gly162Ser
XM_006719434.1:c.484G>A	XP_006719497.1:p.Gly162Ser
XM_011538413.1:c.470-33G>A	XP_011536715.1:n.470-33G>A
XM_011538414.1:c.484G>A	XP_011536716.1:p.Gly162Ser
XR_944557.1:n.560-33G>A
XR_944558.1:n.560-33G>A
NM_001032409.2:c.484G>A	NP_001027581.1:p.Gly162Ser
NM_001320151.1:c.484G>A	NP_001307080.1:p.Gly162Ser
NM_002534.3:c.484G>A	NP_002525.2:p.Gly162Ser
NM_016816.3:c.484G>A	NP_058132.2:p.Gly162Ser
XM_006719434.2:c.484G>A	XP_006719497.1:p.Gly162Ser
XM_011538413.2:c.470-33G>A	XP_011536715.1:n.470-33G>A
XM_017019361.2:c.470-33G>A	XP_016874850.1:n.470-33G>A
XM_017019362.1:c.28-33G>A	XP_016874851.1:n.28-33G>A
XR_944558.2:n.554-33G>A
NM_016816.4:c.484G>A MANE Select	NP_058132.2:p.Gly162Ser
NM_001032409.3:c.484G>A	NP_001027581.1:p.Gly162Ser
NM_001320151.2:c.484G>A	NP_001307080.1:p.Gly162Ser
NM_002534.4:c.484G>A	NP_002525.2:p.Gly162Ser