Canonical Allele Identifier: CA1203049873
Gene: NOS1AP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.162199628_162199650delinsGTGTGTGTGTGTGTCTGTGTGTA , CM000663.2:g.162199628_162199650delinsGTGTGTGTGTGTGTCTGTGTGTA GRCh38
NC_000001.10:g.162169418_162169440delinsGTGTGTGTGTGTGTCTGTGTGTA , CM000663.1:g.162169418_162169440delinsGTGTGTGTGTGTGTCTGTGTGTA GRCh37
NC_000001.9:g.160436042_160436064delinsGTGTGTGTGTGTGTCTGTGTGTA NCBI36
NG_015979.1:g.134838_134860delinsGTGTGTGTGTGTGTCTGTGTGTA
NG_015979.2:g.134838_134860delinsGTGTGTGTGTGTGTCTGTGTGTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000361897.10:c.177+45152_177+45174delinsGTGTGTGTGTGTGTCTGTGTGTA MANE Select ENSP00000355133.5:n.177+45152_177+45174delinsGTGTGTGTGTGTGTCT...
ENST00000361897.9:c.177+45152_177+45174delinsGTGTGTGTGTGTGTCTGTGTGTA ENSP00000355133.5:n.177+45152_177+45174delinsGTGTGTGTGTGTGTCT...
ENST00000430120.3:c.177+45152_177+45174delinsGTGTGTGTGTGTGTCTGTGTGTA ENSP00000396713.3:n.177+45152_177+45174delinsGTGTGTGTGTGTGTCT...
ENST00000530878.5:c.177+45152_177+45174delinsGTGTGTGTGTGTGTCTGTGTGTA ENSP00000431586.1:n.177+45152_177+45174delinsGTGTGTGTGTGTGTCT...
NM_001164757.1:c.177+45152_177+45174delinsGTGTGTGTGTGTGTCTGTGTGTA NP_001158229.1:n.177+45152_177+45174delinsGTGTGTGTGTGTGTCTGTG...
NM_014697.2:c.177+45152_177+45174delinsGTGTGTGTGTGTGTCTGTGTGTA NP_055512.1:n.177+45152_177+45174delinsGTGTGTGTGTGTGTCTGTGTGT...
NM_014697.3:c.177+45152_177+45174delinsGTGTGTGTGTGTGTCTGTGTGTA MANE Select NP_055512.1:n.177+45152_177+45174delinsGTGTGTGTGTGTGTCTGTGTGT...
NM_001164757.2:c.177+45152_177+45174delinsGTGTGTGTGTGTGTCTGTGTGTA NP_001158229.1:n.177+45152_177+45174delinsGTGTGTGTGTGTGTCTGTG...