Canonical Allele Identifier: CA2066036843
Gene: NOS1 HGNC NCBI

Linked Data

dbSNP Id: rs1876163061
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117342556_117342563del , CM000674.2:g.117342556_117342563del GRCh38
NC_000012.11:g.117780361_117780368del , CM000674.1:g.117780361_117780368del GRCh37
NC_000012.10:g.116264744_116264751del NCBI36
NG_011991.2:g.24216_24223del

Transcript Alleles

HGVS Amino-acid Change
ENST00000317775.11:c.-420-11073_-420-11066del MANE Select ENSP00000320758.6:n.-420-11073_-420-11066del
ENST00000317775.10:c.-420-11073_-420-11066del ENSP00000320758.6:n.-420-11073_-420-11066del
ENST00000549189.1:n.471-11073_471-11066del
ENST00000618760.4:c.-420-11073_-420-11066del ENSP00000477999.1:n.-420-11073_-420-11066del
NM_000620.4:c.-420-11073_-420-11066del NP_000611.1:n.-420-11073_-420-11066del
NM_001204218.1:c.-420-11073_-420-11066del NP_001191147.1:n.-420-11073_-420-11066del
XM_011538398.1:c.-420-11073_-420-11066del XP_011536700.1:n.-420-11073_-420-11066del
NM_000620.5:c.-420-11073_-420-11066del MANE Select NP_000611.1:n.-420-11073_-420-11066del
NM_001204218.2:c.-420-11073_-420-11066del NP_001191147.1:n.-420-11073_-420-11066del
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