Canonical Allele Identifier: CA2065974594
Gene: NOS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117215033G= , CM000674.2:g.117215033G= GRCh38
NC_000012.11:g.117652838G= , CM000674.1:g.117652838G= GRCh37
NC_000012.10:g.116137221G= NCBI36
NG_011991.2:g.151745C=

Transcript Alleles

HGVS Amino-acid change
ENST00000317775.11:c.*276C= MANE Select ENSP00000320758.6:n.*276C=
ENST00000317775.10:c.*276C= ENSP00000320758.6:n.*276C=
ENST00000618760.4:c.*276C= ENSP00000477999.1:n.*276C=
NM_000620.4:c.*276C= NP_000611.1:n.*276C=
NM_001204213.1:c.*276C= NP_001191142.1:n.*276C=
NM_001204214.1:c.*276C= NP_001191143.1:n.*276C=
NM_001204218.1:c.*276C= NP_001191147.1:n.*276C=
XM_011538398.1:c.*276C= XP_011536700.1:n.*276C=
NM_000620.5:c.*276C= MANE Select NP_000611.1:n.*276C=
NM_001204213.2:c.*276C= NP_001191142.1:n.*276C=
NM_001204214.2:c.*276C= NP_001191143.1:n.*276C=
NM_001204218.2:c.*276C= NP_001191147.1:n.*276C=