Canonical Allele Identifier: CA2066019596
Gene: NOS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117329740C= , CM000674.2:g.117329740C= GRCh38
NC_000012.11:g.117767545C= , CM000674.1:g.117767545C= GRCh37
NC_000012.10:g.116251928C= NCBI36
NG_011991.2:g.37038G=

Transcript Alleles

HGVS Amino-acid change
ENST00000317775.11:c.725+605G= MANE Select ENSP00000320758.6:n.725+605G=
ENST00000317775.10:c.725+605G= ENSP00000320758.6:n.725+605G=
ENST00000338101.8:c.725+605G= ENSP00000337459.4:n.725+605G=
ENST00000344089.4:c.722+605G= ENSP00000339862.4:n.722+605G=
ENST00000618760.4:c.725+605G= ENSP00000477999.1:n.725+605G=
NM_000620.4:c.725+605G= NP_000611.1:n.725+605G=
NM_001204218.1:c.725+605G= NP_001191147.1:n.725+605G=
XM_011538398.1:c.725+605G= XP_011536700.1:n.725+605G=
NM_000620.5:c.725+605G= MANE Select NP_000611.1:n.725+605G=
NM_001204218.2:c.725+605G= NP_001191147.1:n.725+605G=