Canonical Allele Identifier: CA2066004888

Gene: NOS1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.117313767G= , CM000674.2:g.117313767G=	GRCh38
NC_000012.11:g.117751572G= , CM000674.1:g.117751572G=	GRCh37
NC_000012.10:g.116235955G=	NCBI36
NG_011991.2:g.53011C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317775.11:c.726-2175C= MANE Select	ENSP00000320758.6:n.726-2175C=
ENST00000317775.10:c.726-2175C=	ENSP00000320758.6:n.726-2175C=
ENST00000338101.8:c.726-2175C=	ENSP00000337459.4:n.726-2175C=
ENST00000344089.4:c.723-2175C=	ENSP00000339862.4:n.723-2175C=
ENST00000618760.4:c.726-2175C=	ENSP00000477999.1:n.726-2175C=
NM_000620.4:c.726-2175C=	NP_000611.1:n.726-2175C=
NM_001204218.1:c.726-2175C=	NP_001191147.1:n.726-2175C=
XM_011538398.1:c.726-2175C=	XP_011536700.1:n.726-2175C=
NM_000620.5:c.726-2175C= MANE Select	NP_000611.1:n.726-2175C=
NM_001204218.2:c.726-2175C=	NP_001191147.1:n.726-2175C=