Canonical Allele Identifier: CA2066033169
Gene: NOS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117339710G= , CM000674.2:g.117339710G= GRCh38
NC_000012.11:g.117777515G= , CM000674.1:g.117777515G= GRCh37
NC_000012.10:g.116261898G= NCBI36
NG_011991.2:g.27068C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000317775.11:c.-420-8221C= MANE Select ENSP00000320758.6:n.-420-8221C=
ENST00000317775.10:c.-420-8221C= ENSP00000320758.6:n.-420-8221C=
ENST00000549189.1:n.471-8221C=
ENST00000618760.4:c.-420-8221C= ENSP00000477999.1:n.-420-8221C=
NM_000620.4:c.-420-8221C= NP_000611.1:n.-420-8221C=
NM_001204218.1:c.-420-8221C= NP_001191147.1:n.-420-8221C=
XM_011538398.1:c.-420-8221C= XP_011536700.1:n.-420-8221C=
NM_000620.5:c.-420-8221C= MANE Select NP_000611.1:n.-420-8221C=
NM_001204218.2:c.-420-8221C= NP_001191147.1:n.-420-8221C=
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