Canonical Allele Identifier: CA2066032954
Gene: NOS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117339517T= , CM000674.2:g.117339517T= GRCh38
NC_000012.11:g.117777322T= , CM000674.1:g.117777322T= GRCh37
NC_000012.10:g.116261705T= NCBI36
NG_011991.2:g.27261A=

Transcript Alleles

HGVS Amino-acid change
ENST00000317775.11:c.-420-8028A= MANE Select ENSP00000320758.6:n.-420-8028A=
ENST00000317775.10:c.-420-8028A= ENSP00000320758.6:n.-420-8028A=
ENST00000549189.1:n.471-8028A=
ENST00000618760.4:c.-420-8028A= ENSP00000477999.1:n.-420-8028A=
NM_000620.4:c.-420-8028A= NP_000611.1:n.-420-8028A=
NM_001204218.1:c.-420-8028A= NP_001191147.1:n.-420-8028A=
XM_011538398.1:c.-420-8028A= XP_011536700.1:n.-420-8028A=
NM_000620.5:c.-420-8028A= MANE Select NP_000611.1:n.-420-8028A=
NM_001204218.2:c.-420-8028A= NP_001191147.1:n.-420-8028A=