Canonical Allele Identifier: CA1752467009
Gene: NOS3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150992478_150992479delinsCA , CM000669.2:g.150992478_150992479delinsCA GRCh38
NC_000007.13:g.150689566_150689567delinsCA , CM000669.1:g.150689566_150689567delinsCA GRCh37
NC_000007.12:g.150320499_150320500delinsCA NCBI36
NG_011992.1:g.6420_6421delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000297494.8:c.-52+1178_-52+1179delinsCA MANE Select ENSP00000297494.3:n.-52+1178_-52+1179delinsCA
ENST00000297494.7:c.-52+1178_-52+1179delinsCA ENSP00000297494.3:n.-52+1178_-52+1179delinsCA
ENST00000461406.5:c.-149+1178_-149+1179delinsCA ENSP00000417143.1:n.-149+1178_-149+1179delinsCA
NM_000603.4:c.-52+1178_-52+1179delinsCA NP_000594.2:n.-52+1178_-52+1179delinsCA
NM_000603.5:c.-52+1178_-52+1179delinsCA MANE Select NP_000594.2:n.-52+1178_-52+1179delinsCA