Canonical Allele Identifier: CA2066032767
Gene: NOS1 HGNC NCBI

Linked Data

dbSNP Id: rs1875990542
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117339388_117339391del , CM000674.2:g.117339388_117339391del GRCh38
NC_000012.11:g.117777193_117777196del , CM000674.1:g.117777193_117777196del GRCh37
NC_000012.10:g.116261576_116261579del NCBI36
NG_011991.2:g.27388_27391del

Transcript Alleles

HGVS Amino-acid change
ENST00000317775.11:c.-420-7901_-420-7898del MANE Select ENSP00000320758.6:n.-420-7901_-420-7898de...
ENST00000317775.10:c.-420-7901_-420-7898del ENSP00000320758.6:n.-420-7901_-420-7898de...
ENST00000549189.1:n.471-7901_471-7898del
ENST00000618760.4:c.-420-7901_-420-7898del ENSP00000477999.1:n.-420-7901_-420-7898de...
NM_000620.4:c.-420-7901_-420-7898del NP_000611.1:n.-420-7901_-420-7898del
NM_001204218.1:c.-420-7901_-420-7898del NP_001191147.1:n.-420-7901_-420-7898del
XM_011538398.1:c.-420-7901_-420-7898del XP_011536700.1:n.-420-7901_-420-7898del
NM_000620.5:c.-420-7901_-420-7898del MANE Select NP_000611.1:n.-420-7901_-420-7898del
NM_001204218.2:c.-420-7901_-420-7898del NP_001191147.1:n.-420-7901_-420-7898del
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