Canonical Allele Identifier: CA2518410912

Gene: NOS3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150992620_150992621insCCCCCCCCCCCCCCCC , CM000669.2:g.150992620_150992621insCCCCCCCCCCCCCCCC	GRCh38
NC_000007.13:g.150689708_150689709insCCCCCCCCCCCCCCCC , CM000669.1:g.150689708_150689709insCCCCCCCCCCCCCCCC	GRCh37
NC_000007.12:g.150320641_150320642insCCCCCCCCCCCCCCCC	NCBI36
NG_011992.1:g.6562_6563insCCCCCCCCCCCCCCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297494.8:c.-51-1133_-51-1132insCCCCCCCCCCCCCCCC MANE Select	ENSP00000297494.3:n.-51-1133_-51-1132insCCCCCCCCCCCCCCCC
ENST00000297494.7:c.-51-1133_-51-1132insCCCCCCCCCCCCCCCC	ENSP00000297494.3:n.-51-1133_-51-1132insCCCCCCCCCCCCCCCC
ENST00000461406.5:c.-149+1320_-149+1321insCCCCCCCCCCCCCCCC	ENSP00000417143.1:n.-149+1320_-149+1321insCCCCCCCCCCCCCCCC
NM_000603.4:c.-51-1133_-51-1132insCCCCCCCCCCCCCCCC	NP_000594.2:n.-51-1133_-51-1132insCCCCCCCCCCCCCCCC
NM_000603.5:c.-51-1133_-51-1132insCCCCCCCCCCCCCCCC MANE Select	NP_000594.2:n.-51-1133_-51-1132insCCCCCCCCCCCCCCCC