Canonical Allele Identifier: CA2065994014

Gene: NOS1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.117300538C= , CM000674.2:g.117300538C=	GRCh38
NC_000012.11:g.117738343C= , CM000674.1:g.117738343C=	GRCh37
NC_000012.10:g.116222726C=	NCBI36
NG_011991.2:g.66240G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000317775.11:c.853-10112G= MANE Select	ENSP00000320758.6:n.853-10112G=
ENST00000317775.10:c.853-10112G=	ENSP00000320758.6:n.853-10112G=
ENST00000338101.8:c.853-10112G=	ENSP00000337459.4:n.853-10112G=
ENST00000344089.4:c.850-10112G=	ENSP00000339862.4:n.850-10112G=
ENST00000618760.4:c.853-10112G=	ENSP00000477999.1:n.853-10112G=
NM_000620.4:c.853-10112G=	NP_000611.1:n.853-10112G=
NM_001204213.1:c.-157+1478G=	NP_001191142.1:n.-157+1478G=
NM_001204214.1:c.-157+1478G=	NP_001191143.1:n.-157+1478G=
NM_001204218.1:c.853-10112G=	NP_001191147.1:n.853-10112G=
XM_011538398.1:c.853-10112G=	XP_011536700.1:n.853-10112G=
NM_000620.5:c.853-10112G= MANE Select	NP_000611.1:n.853-10112G=
NM_001204213.2:c.-157+1478G=	NP_001191142.1:n.-157+1478G=
NM_001204214.2:c.-157+1478G=	NP_001191143.1:n.-157+1478G=
NM_001204218.2:c.853-10112G=	NP_001191147.1:n.853-10112G=