Canonical Allele Identifier: CA2065974615
Gene: NOS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117215038T= , CM000674.2:g.117215038T= GRCh38
NC_000012.11:g.117652843T= , CM000674.1:g.117652843T= GRCh37
NC_000012.10:g.116137226T= NCBI36
NG_011991.2:g.151740A=

Transcript Alleles

HGVS Amino-acid change
ENST00000317775.11:c.*271A= MANE Select ENSP00000320758.6:n.*271A=
ENST00000317775.10:c.*271A= ENSP00000320758.6:n.*271A=
ENST00000618760.4:c.*271A= ENSP00000477999.1:n.*271A=
NM_000620.4:c.*271A= NP_000611.1:n.*271A=
NM_001204213.1:c.*271A= NP_001191142.1:n.*271A=
NM_001204214.1:c.*271A= NP_001191143.1:n.*271A=
NM_001204218.1:c.*271A= NP_001191147.1:n.*271A=
XM_011538398.1:c.*271A= XP_011536700.1:n.*271A=
NM_000620.5:c.*271A= MANE Select NP_000611.1:n.*271A=
NM_001204213.2:c.*271A= NP_001191142.1:n.*271A=
NM_001204214.2:c.*271A= NP_001191143.1:n.*271A=
NM_001204218.2:c.*271A= NP_001191147.1:n.*271A=