Canonical Allele Identifier: CA1752440882

Gene: NOS3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151010998_151011001delinsGGAA , CM000669.2:g.151010998_151011001delinsGGAA	GRCh38
NC_000007.13:g.150708086_150708089delinsGGAA , CM000669.1:g.150708086_150708089delinsGGAA	GRCh37
NC_000007.12:g.150339019_150339022delinsGGAA	NCBI36
NG_011992.1:g.24940_24943delinsGGAA
NG_030317.1:g.18499_18502delinsTTCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000297494.8:c.2984+12_2984+15delinsGGAA MANE Select	ENSP00000297494.3:n.2984+12_2984+15delinsGGAA
ENST00000297494.7:c.2984+12_2984+15delinsGGAA	ENSP00000297494.3:n.2984+12_2984+15delinsGGAA
ENST00000461406.5:c.2366+12_2366+15delinsGGAA	ENSP00000417143.1:n.2366+12_2366+15delinsGGAA
ENST00000468293.5:n.467+12_467+15delinsGGAA
ENST00000475017.1:c.865+12_865+15delinsGGAA
ENST00000477227.1:n.363+12_363+15delinsGGAA
NM_000603.4:c.2984+12_2984+15delinsGGAA	NP_000594.2:n.2984+12_2984+15delinsGGAA
NM_000603.5:c.2984+12_2984+15delinsGGAA MANE Select	NP_000594.2:n.2984+12_2984+15delinsGGAA