Canonical Allele Identifier: CA2066032882

Gene: NOS1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.117339473_117339474delinsAC , CM000674.2:g.117339473_117339474delinsAC	GRCh38
NC_000012.11:g.117777278_117777279delinsAC , CM000674.1:g.117777278_117777279delinsAC	GRCh37
NC_000012.10:g.116261661_116261662delinsAC	NCBI36
NG_011991.2:g.27304_27305delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317775.11:c.-420-7985_-420-7984delinsGT MANE Select	ENSP00000320758.6:n.-420-7985_-420-7984delinsGT
ENST00000317775.10:c.-420-7985_-420-7984delinsGT	ENSP00000320758.6:n.-420-7985_-420-7984delinsGT
ENST00000549189.1:n.471-7985_471-7984delinsGT
ENST00000618760.4:c.-420-7985_-420-7984delinsGT	ENSP00000477999.1:n.-420-7985_-420-7984delinsGT
NM_000620.4:c.-420-7985_-420-7984delinsGT	NP_000611.1:n.-420-7985_-420-7984delinsGT
NM_001204218.1:c.-420-7985_-420-7984delinsGT	NP_001191147.1:n.-420-7985_-420-7984delinsGT
XM_011538398.1:c.-420-7985_-420-7984delinsGT	XP_011536700.1:n.-420-7985_-420-7984delinsGT
NM_000620.5:c.-420-7985_-420-7984delinsGT MANE Select	NP_000611.1:n.-420-7985_-420-7984delinsGT
NM_001204218.2:c.-420-7985_-420-7984delinsGT	NP_001191147.1:n.-420-7985_-420-7984delinsGT