Canonical Allele Identifier: CA1752441902

Gene: NOS3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151001867_151001868delinsCG , CM000669.2:g.151001867_151001868delinsCG	GRCh38
NC_000007.13:g.150698955_150698956delinsCG , CM000669.1:g.150698955_150698956delinsCG	GRCh37
NC_000007.12:g.150329888_150329889delinsCG	NCBI36
NG_011992.1:g.15809_15810delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297494.8:c.1549_1550delinsCG MANE Select	ENSP00000297494.3:p.Arg517=
ENST00000297494.7:c.1549_1550delinsCG	ENSP00000297494.3:p.Arg517=
ENST00000460603.1:n.1_2delinsCG
ENST00000461406.5:c.931_932delinsCG	ENSP00000417143.1:p.Arg311=
ENST00000467517.1:c.1549_1550delinsCG	ENSP00000420551.1:p.Arg517=
ENST00000484524.5:c.1549_1550delinsCG	ENSP00000420215.1:p.Arg517=
NM_000603.4:c.1549_1550delinsCG	NP_000594.2:p.Arg517=
NM_001160109.1:c.1549_1550delinsCG	NP_001153581.1:p.Arg517=
NM_001160110.1:c.1549_1550delinsCG	NP_001153582.1:p.Arg517=
NM_001160111.1:c.1549_1550delinsCG	NP_001153583.1:p.Arg517=
XM_006716002.2:c.1549_1550delinsCG	XP_006716065.1:p.Arg517=
NM_000603.5:c.1549_1550delinsCG MANE Select	NP_000594.2:p.Arg517=
NM_001160109.2:c.1549_1550delinsCG	NP_001153581.1:p.Arg517=