Canonical Allele Identifier: CA1752467238

Gene: NOS3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150992989_150992991delinsGCC , CM000669.2:g.150992989_150992991delinsGCC	GRCh38
NC_000007.13:g.150690077_150690079delinsGCC , CM000669.1:g.150690077_150690079delinsGCC	GRCh37
NC_000007.12:g.150321010_150321012delinsGCC	NCBI36
NG_011992.1:g.6931_6933delinsGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297494.8:c.-51-764_-51-762delinsGCC MANE Select	ENSP00000297494.3:n.-51-764_-51-762delinsGCC
ENST00000297494.7:c.-51-764_-51-762delinsGCC	ENSP00000297494.3:n.-51-764_-51-762delinsGCC
ENST00000461406.5:c.-149+1689_-149+1691delinsGCC	ENSP00000417143.1:n.-149+1689_-149+1691delinsGCC
NM_000603.4:c.-51-764_-51-762delinsGCC	NP_000594.2:n.-51-764_-51-762delinsGCC
NM_000603.5:c.-51-764_-51-762delinsGCC MANE Select	NP_000594.2:n.-51-764_-51-762delinsGCC