Canonical Allele Identifier: CA2066032897
Gene: NOS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117339487A= , CM000674.2:g.117339487A= GRCh38
NC_000012.11:g.117777292A= , CM000674.1:g.117777292A= GRCh37
NC_000012.10:g.116261675A= NCBI36
NG_011991.2:g.27291T=

Transcript Alleles

HGVS Amino-acid change
ENST00000317775.11:c.-420-7998T= MANE Select ENSP00000320758.6:n.-420-7998T=
ENST00000317775.10:c.-420-7998T= ENSP00000320758.6:n.-420-7998T=
ENST00000549189.1:n.471-7998T=
ENST00000618760.4:c.-420-7998T= ENSP00000477999.1:n.-420-7998T=
NM_000620.4:c.-420-7998T= NP_000611.1:n.-420-7998T=
NM_001204218.1:c.-420-7998T= NP_001191147.1:n.-420-7998T=
XM_011538398.1:c.-420-7998T= XP_011536700.1:n.-420-7998T=
NM_000620.5:c.-420-7998T= MANE Select NP_000611.1:n.-420-7998T=
NM_001204218.2:c.-420-7998T= NP_001191147.1:n.-420-7998T=