Canonical Allele Identifier: CA2066019582
Gene: NOS1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117329724_117329725delinsCT , CM000674.2:g.117329724_117329725delinsCT GRCh38
NC_000012.11:g.117767529_117767530delinsCT , CM000674.1:g.117767529_117767530delinsCT GRCh37
NC_000012.10:g.116251912_116251913delinsCT NCBI36
NG_011991.2:g.37053_37054delinsAG

Transcript Alleles

HGVS Amino-acid change
ENST00000317775.11:c.725+620_725+621delinsAG MANE Select ENSP00000320758.6:n.725+620_725+621delins...
ENST00000317775.10:c.725+620_725+621delinsAG ENSP00000320758.6:n.725+620_725+621delins...
ENST00000338101.8:c.725+620_725+621delinsAG ENSP00000337459.4:n.725+620_725+621delins...
ENST00000344089.4:c.722+620_722+621delinsAG ENSP00000339862.4:n.722+620_722+621delins...
ENST00000618760.4:c.725+620_725+621delinsAG ENSP00000477999.1:n.725+620_725+621delins...
NM_000620.4:c.725+620_725+621delinsAG NP_000611.1:n.725+620_725+621delinsAG
NM_001204218.1:c.725+620_725+621delinsAG NP_001191147.1:n.725+620_725+621delinsAG
XM_011538398.1:c.725+620_725+621delinsAG XP_011536700.1:n.725+620_725+621delinsAG
NM_000620.5:c.725+620_725+621delinsAG MANE Select NP_000611.1:n.725+620_725+621delinsAG
NM_001204218.2:c.725+620_725+621delinsAG NP_001191147.1:n.725+620_725+621delinsAG
Search 100 bp 5'
Search 100 bp 3'