Canonical Allele Identifier: CA607668950
Gene: NOS1 HGNC NCBI

Linked Data

dbSNP Id: rs1448891612

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117339535del , CM000674.2:g.117339535del GRCh38
NC_000012.11:g.117777340del , CM000674.1:g.117777340del GRCh37
NC_000012.10:g.116261723del NCBI36
NG_011991.2:g.27243del

Transcript Alleles

HGVS Amino-acid change
ENST00000317775.11:c.-420-8046del MANE Select ENSP00000320758.6:n.-420-8046del
ENST00000317775.10:c.-420-8046del ENSP00000320758.6:n.-420-8046del
ENST00000549189.1:n.471-8046del
ENST00000618760.4:c.-420-8046del ENSP00000477999.1:n.-420-8046del
NM_000620.4:c.-420-8046del NP_000611.1:n.-420-8046del
NM_001204218.1:c.-420-8046del NP_001191147.1:n.-420-8046del
XM_011538398.1:c.-420-8046del XP_011536700.1:n.-420-8046del
NM_000620.5:c.-420-8046del MANE Select NP_000611.1:n.-420-8046del
NM_001204218.2:c.-420-8046del NP_001191147.1:n.-420-8046del