Canonical Allele Identifier: CA2066036189

Gene: NOS1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.117342093_117342094delinsCA , CM000674.2:g.117342093_117342094delinsCA	GRCh38
NC_000012.11:g.117779898_117779899delinsCA , CM000674.1:g.117779898_117779899delinsCA	GRCh37
NC_000012.10:g.116264281_116264282delinsCA	NCBI36
NG_011991.2:g.24684_24685delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317775.11:c.-420-10605_-420-10604delinsTG MANE Select	ENSP00000320758.6:n.-420-10605_-420-10604delinsTG
ENST00000317775.10:c.-420-10605_-420-10604delinsTG	ENSP00000320758.6:n.-420-10605_-420-10604delinsTG
ENST00000549189.1:n.471-10605_471-10604delinsTG
ENST00000618760.4:c.-420-10605_-420-10604delinsTG	ENSP00000477999.1:n.-420-10605_-420-10604delinsTG
NM_000620.4:c.-420-10605_-420-10604delinsTG	NP_000611.1:n.-420-10605_-420-10604delinsTG
NM_001204218.1:c.-420-10605_-420-10604delinsTG	NP_001191147.1:n.-420-10605_-420-10604delinsTG
XM_011538398.1:c.-420-10605_-420-10604delinsTG	XP_011536700.1:n.-420-10605_-420-10604delinsTG
NM_000620.5:c.-420-10605_-420-10604delinsTG MANE Select	NP_000611.1:n.-420-10605_-420-10604delinsTG
NM_001204218.2:c.-420-10605_-420-10604delinsTG	NP_001191147.1:n.-420-10605_-420-10604delinsTG