Canonical Allele Identifier: CA386814256

Gene: OAS1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.112931878G>T , CM000674.2:g.112931878G>T	GRCh38
NC_000012.11:g.113369683G>T , CM000674.1:g.113369683G>T	GRCh37
NC_000012.10:g.111854066G>T	NCBI36
NG_011530.2:g.29945G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000540589.3:c.1168G>T	ENSP00000474083.2:p.Val390Leu
ENST00000551241.6:c.1039G>T	ENSP00000448790.1:p.Val347Leu
ENST00000552526.2:c.1083G>T	ENSP00000475139.2:p.Arg361Ser
ENST00000540589.2:c.131G>T
ENST00000551241.5:c.1039G>T	ENSP00000448790.1:p.Val347Leu
ENST00000552526.1:c.45G>T	ENSP00000475139.1:p.Arg15Ser
XM_011538414.1:c.1039G>T	XP_011536716.1:p.Val347Leu
NM_001320151.1:c.1039G>T	NP_001307080.1:p.Val347Leu
NM_001320151.2:c.1039G>T	NP_001307080.1:p.Val347Leu