Canonical Allele Identifier: CA1203049803
Gene: NOS1AP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.162199526_162199531delinsCAAGAA , CM000663.2:g.162199526_162199531delinsCAAGAA GRCh38
NC_000001.10:g.162169316_162169321delinsCAAGAA , CM000663.1:g.162169316_162169321delinsCAAGAA GRCh37
NC_000001.9:g.160435940_160435945delinsCAAGAA NCBI36
NG_015979.1:g.134736_134741delinsCAAGAA
NG_015979.2:g.134736_134741delinsCAAGAA

Transcript Alleles

HGVS Amino-acid change
ENST00000361897.10:c.177+45050_177+45055delinsCAAGAA MANE Select ENSP00000355133.5:n.177+45050_177+45055de...
ENST00000361897.9:c.177+45050_177+45055delinsCAAGAA ENSP00000355133.5:n.177+45050_177+45055de...
ENST00000430120.3:c.177+45050_177+45055delinsCAAGAA ENSP00000396713.3:n.177+45050_177+45055de...
ENST00000530878.5:c.177+45050_177+45055delinsCAAGAA ENSP00000431586.1:n.177+45050_177+45055de...
NM_001164757.1:c.177+45050_177+45055delinsCAAGAA NP_001158229.1:n.177+45050_177+45055delin...
NM_014697.2:c.177+45050_177+45055delinsCAAGAA NP_055512.1:n.177+45050_177+45055delinsCA...
NM_014697.3:c.177+45050_177+45055delinsCAAGAA MANE Select NP_055512.1:n.177+45050_177+45055delinsCA...
NM_001164757.2:c.177+45050_177+45055delinsCAAGAA NP_001158229.1:n.177+45050_177+45055delin...