Canonical Allele Identifier: CA1752467085

Gene: NOS3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150992624_150992627delinsCAGG , CM000669.2:g.150992624_150992627delinsCAGG	GRCh38
NC_000007.13:g.150689712_150689715delinsCAGG , CM000669.1:g.150689712_150689715delinsCAGG	GRCh37
NC_000007.12:g.150320645_150320648delinsCAGG	NCBI36
NG_011992.1:g.6566_6569delinsCAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297494.8:c.-51-1129_-51-1126delinsCAGG MANE Select	ENSP00000297494.3:n.-51-1129_-51-1126delinsCAGG
ENST00000297494.7:c.-51-1129_-51-1126delinsCAGG	ENSP00000297494.3:n.-51-1129_-51-1126delinsCAGG
ENST00000461406.5:c.-149+1324_-149+1327delinsCAGG	ENSP00000417143.1:n.-149+1324_-149+1327delinsCAGG
NM_000603.4:c.-51-1129_-51-1126delinsCAGG	NP_000594.2:n.-51-1129_-51-1126delinsCAGG
NM_000603.5:c.-51-1129_-51-1126delinsCAGG MANE Select	NP_000594.2:n.-51-1129_-51-1126delinsCAGG