Canonical Allele Identifier: CA2063956545
Gene: OAS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.112927816A= , CM000674.2:g.112927816A= GRCh38
NC_000012.11:g.113365621A= , CM000674.1:g.113365621A= GRCh37
NC_000012.10:g.111850004A= NCBI36
NG_011530.2:g.25883A=

Transcript Alleles

HGVS Amino-acid Change
NM_001320151.1:c.1039-4062A= NP_001307080.1:n.1039-4062A=
NM_001320151.2:c.1039-4062A= NP_001307080.1:n.1039-4062A=
ENST00000540589.2:c.131-4062A=
ENST00000540589.3:c.1168-4062A= ENSP00000474083.2:n.1168-4062A=
ENST00000551241.5:c.1039-4062A= ENSP00000448790.1:n.1039-4062A=
ENST00000551241.6:c.1039-4062A= ENSP00000448790.1:n.1039-4062A=
ENST00000552526.1:c.45-4062A= ENSP00000475139.1:n.45-4062A=
ENST00000552526.2:c.1083-4062A= ENSP00000475139.2:n.1083-4062A=
XM_011538414.1:c.1039-4062A= XP_011536716.1:n.1039-4062A=