Canonical Allele Identifier: CA2066036207

Gene: NOS1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.117342111_117342114delinsCTTT , CM000674.2:g.117342111_117342114delinsCTTT	GRCh38
NC_000012.11:g.117779916_117779919delinsCTTT , CM000674.1:g.117779916_117779919delinsCTTT	GRCh37
NC_000012.10:g.116264299_116264302delinsCTTT	NCBI36
NG_011991.2:g.24664_24667delinsAAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317775.11:c.-420-10625_-420-10622delinsAAAG MANE Select	ENSP00000320758.6:n.-420-10625_-420-10622delinsAAAG
ENST00000317775.10:c.-420-10625_-420-10622delinsAAAG	ENSP00000320758.6:n.-420-10625_-420-10622delinsAAAG
ENST00000549189.1:n.471-10625_471-10622delinsAAAG
ENST00000618760.4:c.-420-10625_-420-10622delinsAAAG	ENSP00000477999.1:n.-420-10625_-420-10622delinsAAAG
NM_000620.4:c.-420-10625_-420-10622delinsAAAG	NP_000611.1:n.-420-10625_-420-10622delinsAAAG
NM_001204218.1:c.-420-10625_-420-10622delinsAAAG	NP_001191147.1:n.-420-10625_-420-10622delinsAAAG
XM_011538398.1:c.-420-10625_-420-10622delinsAAAG	XP_011536700.1:n.-420-10625_-420-10622delinsAAAG
NM_000620.5:c.-420-10625_-420-10622delinsAAAG MANE Select	NP_000611.1:n.-420-10625_-420-10622delinsAAAG
NM_001204218.2:c.-420-10625_-420-10622delinsAAAG	NP_001191147.1:n.-420-10625_-420-10622delinsAAAG