Canonical Allele Identifier: CA1752443014

Gene: NOS3 ATG9B

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151012483G= , CM000669.2:g.151012483G=	GRCh38
NC_000007.13:g.150709571G= , CM000669.1:g.150709571G=	GRCh37
NC_000007.12:g.150340504G=	NCBI36
NG_011992.1:g.26425G=
NG_030317.1:g.17017C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297494.8:c.3106+11G= (NOS3) MANE Select	ENSP00000297494.3:n.3106+11G=
ENST00000639579.1:c.*1452C= (ATG9B)	ENSP00000491504.1:n.*1452C=
ENST00000297494.7:c.3106+11G= (NOS3)	ENSP00000297494.3:n.3106+11G=
ENST00000461406.5:c.2488+11G= (NOS3)	ENSP00000417143.1:n.2488+11G=
ENST00000468293.5:n.589+11G= (NOS3)
ENST00000475454.1:n.67+11G= (NOS3)
ENST00000477227.1:n.485+11G= (NOS3)
ENST00000498521.2:n.161-33C= (ATG9B)
ENST00000605952.5:c.*1452C= (ATG9B)	ENSP00000475737.2:n.*1452C=
NM_000603.4:c.3106+11G= (NOS3)	NP_000594.2:n.3106+11G=
NM_173681.5:c.*1452C= (ATG9B)	NP_775952.4:n.*1452C=
NR_073169.1:n.3566C= (ATG9B)
NR_133652.1:n.4303C= (ATG9B)
NM_000603.5:c.3106+11G= (NOS3) MANE Select	NP_000594.2:n.3106+11G=