Canonical Allele Identifier: CA2066054743

Gene: NOS1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.117357967_117357968delinsAC , CM000674.2:g.117357967_117357968delinsAC	GRCh38
NC_000012.11:g.117795772_117795773delinsAC , CM000674.1:g.117795772_117795773delinsAC	GRCh37
NC_000012.10:g.116280155_116280156delinsAC	NCBI36
NG_011991.2:g.8810_8811delinsGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000317775.11:c.-421+3544_-421+3545delinsGT MANE Select	ENSP00000320758.6:n.-421+3544_-421+3545delinsGT
ENST00000317775.10:c.-421+3544_-421+3545delinsGT	ENSP00000320758.6:n.-421+3544_-421+3545delinsGT
ENST00000477584.1:n.118+3544_118+3545delinsGT
ENST00000549189.1:n.471-26479_471-26478delinsGT
ENST00000618760.4:c.-421+3544_-421+3545delinsGT	ENSP00000477999.1:n.-421+3544_-421+3545delinsGT
NM_000620.4:c.-421+3544_-421+3545delinsGT	NP_000611.1:n.-421+3544_-421+3545delinsGT
NM_001204218.1:c.-421+3544_-421+3545delinsGT	NP_001191147.1:n.-421+3544_-421+3545delinsGT
XM_011538398.1:c.-421+1023_-421+1024delinsGT	XP_011536700.1:n.-421+1023_-421+1024delinsGT
NM_000620.5:c.-421+3544_-421+3545delinsGT MANE Select	NP_000611.1:n.-421+3544_-421+3545delinsGT
NM_001204218.2:c.-421+3544_-421+3545delinsGT	NP_001191147.1:n.-421+3544_-421+3545delinsGT