Canonical Allele Identifier: CA1752446729

Gene: NOS3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151003897G= , CM000669.2:g.151003897G=	GRCh38
NC_000007.13:g.150700985G= , CM000669.1:g.150700985G=	GRCh37
NC_000007.12:g.150331918G=	NCBI36
NG_011992.1:g.17839G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297494.8:c.1752+1593G= MANE Select	ENSP00000297494.3:n.1752+1593G=
ENST00000297494.7:c.1752+1593G=	ENSP00000297494.3:n.1752+1593G=
ENST00000461406.5:c.1134+1593G=	ENSP00000417143.1:n.1134+1593G=
ENST00000467517.1:c.2339G=	ENSP00000420551.1:n.2339G=
ENST00000484524.5:c.2499G=	ENSP00000420215.1:n.2499G=
NM_000603.4:c.1752+1593G=	NP_000594.2:n.1752+1593G=
NM_001160109.1:c.1993G=	NP_001153581.1:n.1993G=
NM_001160110.1:c.2339G=	NP_001153582.1:n.2339G=
NM_001160111.1:c.2499G=	NP_001153583.1:n.2499G=
XM_006716002.2:c.1752+1593G=	XP_006716065.1:n.1752+1593G=
NM_000603.5:c.1752+1593G= MANE Select	NP_000594.2:n.1752+1593G=
NM_001160109.2:c.*202G=	NP_001153581.1:n.*202G=