Canonical Allele Identifier: CA1752470788

Gene: NOS3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150999038C= , CM000669.2:g.150999038C=	GRCh38
NC_000007.13:g.150696126C= , CM000669.1:g.150696126C=	GRCh37
NC_000007.12:g.150327059C=	NCBI36
NG_011992.1:g.12980C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297494.8:c.909C= MANE Select	ENSP00000297494.3:p.Phe303=
ENST00000297494.7:c.909C=	ENSP00000297494.3:p.Phe303=
ENST00000461406.5:c.291C=	ENSP00000417143.1:p.Phe97=
ENST00000467517.1:c.909C=	ENSP00000420551.1:p.Phe303=
ENST00000484524.5:c.909C=	ENSP00000420215.1:p.Phe303=
NM_000603.4:c.909C=	NP_000594.2:p.Phe303=
NM_001160109.1:c.909C=	NP_001153581.1:p.Phe303=
NM_001160110.1:c.909C=	NP_001153582.1:p.Phe303=
NM_001160111.1:c.909C=	NP_001153583.1:p.Phe303=
XM_006716002.2:c.909C=	XP_006716065.1:p.Phe303=
NM_000603.5:c.909C= MANE Select	NP_000594.2:p.Phe303=
NM_001160109.2:c.909C=	NP_001153581.1:p.Phe303=