Canonical Allele Identifier: CA2065974654
Gene: NOS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117215052_117215054delinsAAG , CM000674.2:g.117215052_117215054delinsAAG GRCh38
NC_000012.11:g.117652857_117652859delinsAAG , CM000674.1:g.117652857_117652859delinsAAG GRCh37
NC_000012.10:g.116137240_116137242delinsAAG NCBI36
NG_011991.2:g.151724_151726delinsCTT

Transcript Alleles

HGVS Amino-acid change
ENST00000317775.11:c.*255_*257delinsCTT MANE Select ENSP00000320758.6:n.*255_*257delinsCTT
ENST00000317775.10:c.*255_*257delinsCTT ENSP00000320758.6:n.*255_*257delinsCTT
ENST00000618760.4:c.*255_*257delinsCTT ENSP00000477999.1:n.*255_*257delinsCTT
NM_000620.4:c.*255_*257delinsCTT NP_000611.1:n.*255_*257delinsCTT
NM_001204213.1:c.*255_*257delinsCTT NP_001191142.1:n.*255_*257delinsCTT
NM_001204214.1:c.*255_*257delinsCTT NP_001191143.1:n.*255_*257delinsCTT
NM_001204218.1:c.*255_*257delinsCTT NP_001191147.1:n.*255_*257delinsCTT
XM_011538398.1:c.*255_*257delinsCTT XP_011536700.1:n.*255_*257delinsCTT
NM_000620.5:c.*255_*257delinsCTT MANE Select NP_000611.1:n.*255_*257delinsCTT
NM_001204213.2:c.*255_*257delinsCTT NP_001191142.1:n.*255_*257delinsCTT
NM_001204214.2:c.*255_*257delinsCTT NP_001191143.1:n.*255_*257delinsCTT
NM_001204218.2:c.*255_*257delinsCTT NP_001191147.1:n.*255_*257delinsCTT