Canonical Allele Identifier: CA1203049877

Gene: NOS1AP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162199632_162199650delinsGTGTGTGTGTCTGTGTGTA , CM000663.2:g.162199632_162199650delinsGTGTGTGTGTCTGTGTGTA	GRCh38
NC_000001.10:g.162169422_162169440delinsGTGTGTGTGTCTGTGTGTA , CM000663.1:g.162169422_162169440delinsGTGTGTGTGTCTGTGTGTA	GRCh37
NC_000001.9:g.160436046_160436064delinsGTGTGTGTGTCTGTGTGTA	NCBI36
NG_015979.1:g.134842_134860delinsGTGTGTGTGTCTGTGTGTA
NG_015979.2:g.134842_134860delinsGTGTGTGTGTCTGTGTGTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361897.10:c.177+45156_177+45174delinsGTGTGTGTGTCTGTGTGTA MANE Select	ENSP00000355133.5:n.177+45156_177+45174delinsGTGTGTGTGTCTGTGT...
ENST00000361897.9:c.177+45156_177+45174delinsGTGTGTGTGTCTGTGTGTA	ENSP00000355133.5:n.177+45156_177+45174delinsGTGTGTGTGTCTGTGT...
ENST00000430120.3:c.177+45156_177+45174delinsGTGTGTGTGTCTGTGTGTA	ENSP00000396713.3:n.177+45156_177+45174delinsGTGTGTGTGTCTGTGT...
ENST00000530878.5:c.177+45156_177+45174delinsGTGTGTGTGTCTGTGTGTA	ENSP00000431586.1:n.177+45156_177+45174delinsGTGTGTGTGTCTGTGT...
NM_001164757.1:c.177+45156_177+45174delinsGTGTGTGTGTCTGTGTGTA	NP_001158229.1:n.177+45156_177+45174delinsGTGTGTGTGTCTGTGTGTA...
NM_014697.2:c.177+45156_177+45174delinsGTGTGTGTGTCTGTGTGTA	NP_055512.1:n.177+45156_177+45174delinsGTGTGTGTGTCTGTGTGTA
NM_014697.3:c.177+45156_177+45174delinsGTGTGTGTGTCTGTGTGTA MANE Select	NP_055512.1:n.177+45156_177+45174delinsGTGTGTGTGTCTGTGTGTA
NM_001164757.2:c.177+45156_177+45174delinsGTGTGTGTGTCTGTGTGTA	NP_001158229.1:n.177+45156_177+45174delinsGTGTGTGTGTCTGTGTGTA...