Canonical Allele Identifier: CA2066036401

Gene: NOS1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.117342245_117342246delinsAT , CM000674.2:g.117342245_117342246delinsAT	GRCh38
NC_000012.11:g.117780050_117780051delinsAT , CM000674.1:g.117780050_117780051delinsAT	GRCh37
NC_000012.10:g.116264433_116264434delinsAT	NCBI36
NG_011991.2:g.24532_24533delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317775.11:c.-420-10757_-420-10756delinsAT MANE Select	ENSP00000320758.6:n.-420-10757_-420-10756delinsAT
ENST00000317775.10:c.-420-10757_-420-10756delinsAT	ENSP00000320758.6:n.-420-10757_-420-10756delinsAT
ENST00000549189.1:n.471-10757_471-10756delinsAT
ENST00000618760.4:c.-420-10757_-420-10756delinsAT	ENSP00000477999.1:n.-420-10757_-420-10756delinsAT
NM_000620.4:c.-420-10757_-420-10756delinsAT	NP_000611.1:n.-420-10757_-420-10756delinsAT
NM_001204218.1:c.-420-10757_-420-10756delinsAT	NP_001191147.1:n.-420-10757_-420-10756delinsAT
XM_011538398.1:c.-420-10757_-420-10756delinsAT	XP_011536700.1:n.-420-10757_-420-10756delinsAT
NM_000620.5:c.-420-10757_-420-10756delinsAT MANE Select	NP_000611.1:n.-420-10757_-420-10756delinsAT
NM_001204218.2:c.-420-10757_-420-10756delinsAT	NP_001191147.1:n.-420-10757_-420-10756delinsAT