Canonical Allele Identifier: CA2065993881
Gene: NOS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117300503A= , CM000674.2:g.117300503A= GRCh38
NC_000012.11:g.117738308A= , CM000674.1:g.117738308A= GRCh37
NC_000012.10:g.116222691A= NCBI36
NG_011991.2:g.66275T=

Transcript Alleles

HGVS Amino-acid change
ENST00000317775.11:c.853-10077T= MANE Select ENSP00000320758.6:n.853-10077T=
ENST00000317775.10:c.853-10077T= ENSP00000320758.6:n.853-10077T=
ENST00000338101.8:c.853-10077T= ENSP00000337459.4:n.853-10077T=
ENST00000344089.4:c.850-10077T= ENSP00000339862.4:n.850-10077T=
ENST00000618760.4:c.853-10077T= ENSP00000477999.1:n.853-10077T=
NM_000620.4:c.853-10077T= NP_000611.1:n.853-10077T=
NM_001204213.1:c.-157+1513T= NP_001191142.1:n.-157+1513T=
NM_001204214.1:c.-157+1513T= NP_001191143.1:n.-157+1513T=
NM_001204218.1:c.853-10077T= NP_001191147.1:n.853-10077T=
XM_011538398.1:c.853-10077T= XP_011536700.1:n.853-10077T=
NM_000620.5:c.853-10077T= MANE Select NP_000611.1:n.853-10077T=
NM_001204213.2:c.-157+1513T= NP_001191142.1:n.-157+1513T=
NM_001204214.2:c.-157+1513T= NP_001191143.1:n.-157+1513T=
NM_001204218.2:c.853-10077T= NP_001191147.1:n.853-10077T=