Canonical Allele Identifier: CA2066054914
Gene: NOS1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117358179G= , CM000674.2:g.117358179G= GRCh38
NC_000012.11:g.117795984G= , CM000674.1:g.117795984G= GRCh37
NC_000012.10:g.116280367G= NCBI36
NG_011991.2:g.8599C=

Transcript Alleles

HGVS Amino-acid change
ENST00000317775.11:c.-421+3333C= MANE Select ENSP00000320758.6:n.-421+3333C=
ENST00000317775.10:c.-421+3333C= ENSP00000320758.6:n.-421+3333C=
ENST00000477584.1:n.118+3333C=
ENST00000549189.1:n.471-26690C=
ENST00000618760.4:c.-421+3333C= ENSP00000477999.1:n.-421+3333C=
NM_000620.4:c.-421+3333C= NP_000611.1:n.-421+3333C=
NM_001204218.1:c.-421+3333C= NP_001191147.1:n.-421+3333C=
XM_011538398.1:c.-421+812C= XP_011536700.1:n.-421+812C=
NM_000620.5:c.-421+3333C= MANE Select NP_000611.1:n.-421+3333C=
NM_001204218.2:c.-421+3333C= NP_001191147.1:n.-421+3333C=
Search 100 bp 5'
Search 100 bp 3'