Canonical Allele Identifier: CA2066019576
Gene: NOS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117329722T= , CM000674.2:g.117329722T= GRCh38
NC_000012.11:g.117767527T= , CM000674.1:g.117767527T= GRCh37
NC_000012.10:g.116251910T= NCBI36
NG_011991.2:g.37056A=

Transcript Alleles

HGVS Amino-acid change
ENST00000317775.11:c.725+623A= MANE Select ENSP00000320758.6:n.725+623A=
ENST00000317775.10:c.725+623A= ENSP00000320758.6:n.725+623A=
ENST00000338101.8:c.725+623A= ENSP00000337459.4:n.725+623A=
ENST00000344089.4:c.722+623A= ENSP00000339862.4:n.722+623A=
ENST00000618760.4:c.725+623A= ENSP00000477999.1:n.725+623A=
NM_000620.4:c.725+623A= NP_000611.1:n.725+623A=
NM_001204218.1:c.725+623A= NP_001191147.1:n.725+623A=
XM_011538398.1:c.725+623A= XP_011536700.1:n.725+623A=
NM_000620.5:c.725+623A= MANE Select NP_000611.1:n.725+623A=
NM_001204218.2:c.725+623A= NP_001191147.1:n.725+623A=