Canonical Allele Identifier: CA1752446621

Gene: NOS3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151003811C= , CM000669.2:g.151003811C=	GRCh38
NC_000007.13:g.150700899C= , CM000669.1:g.150700899C=	GRCh37
NC_000007.12:g.150331832C=	NCBI36
NG_011992.1:g.17753C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297494.8:c.1752+1507C= MANE Select	ENSP00000297494.3:n.1752+1507C=
ENST00000297494.7:c.1752+1507C=	ENSP00000297494.3:n.1752+1507C=
ENST00000461406.5:c.1134+1507C=	ENSP00000417143.1:n.1134+1507C=
ENST00000467517.1:c.2253C=	ENSP00000420551.1:n.2253C=
ENST00000484524.5:c.2413C=	ENSP00000420215.1:n.2413C=
NM_000603.4:c.1752+1507C=	NP_000594.2:n.1752+1507C=
NM_001160109.1:c.1907C=	NP_001153581.1:n.1907C=
NM_001160110.1:c.2253C=	NP_001153582.1:n.2253C=
NM_001160111.1:c.2413C=	NP_001153583.1:n.2413C=
XM_006716002.2:c.1752+1507C=	XP_006716065.1:n.1752+1507C=
NM_000603.5:c.1752+1507C= MANE Select	NP_000594.2:n.1752+1507C=
NM_001160109.2:c.*116C=	NP_001153581.1:n.*116C=