Canonical Allele Identifier: CA1752467081

Gene: NOS3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150992620_150992627delinsCACCCAGG , CM000669.2:g.150992620_150992627delinsCACCCAGG	GRCh38
NC_000007.13:g.150689708_150689715delinsCACCCAGG , CM000669.1:g.150689708_150689715delinsCACCCAGG	GRCh37
NC_000007.12:g.150320641_150320648delinsCACCCAGG	NCBI36
NG_011992.1:g.6562_6569delinsCACCCAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297494.8:c.-51-1133_-51-1126delinsCACCCAGG MANE Select	ENSP00000297494.3:n.-51-1133_-51-1126delinsCACCCAGG
ENST00000297494.7:c.-51-1133_-51-1126delinsCACCCAGG	ENSP00000297494.3:n.-51-1133_-51-1126delinsCACCCAGG
ENST00000461406.5:c.-149+1320_-149+1327delinsCACCCAGG	ENSP00000417143.1:n.-149+1320_-149+1327delinsCACCCAGG
NM_000603.4:c.-51-1133_-51-1126delinsCACCCAGG	NP_000594.2:n.-51-1133_-51-1126delinsCACCCAGG
NM_000603.5:c.-51-1133_-51-1126delinsCACCCAGG MANE Select	NP_000594.2:n.-51-1133_-51-1126delinsCACCCAGG