Canonical Allele Identifier: CA31691981

Gene: NOS1AP

Linked Data

• dbSNP Id: rs766338899
• MyVariant Identifiers: chr1:g.162169430_162169431insTCTGTGTGTA (hg19) ; chr1:g.162199640_162199641insTCTGTGTGTA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162199641_162199650dup , CM000663.2:g.162199641_162199650dup	GRCh38
NC_000001.10:g.162169431_162169440dup , CM000663.1:g.162169431_162169440dup	GRCh37
NC_000001.9:g.160436055_160436064dup	NCBI36
NG_015979.1:g.134851_134860dup
NG_015979.2:g.134851_134860dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361897.10:c.177+45165_177+45174dup MANE Select	ENSP00000355133.5:n.177+45165_177+45174dup
ENST00000361897.9:c.177+45165_177+45174dup	ENSP00000355133.5:n.177+45165_177+45174dup
ENST00000430120.3:c.177+45165_177+45174dup	ENSP00000396713.3:n.177+45165_177+45174dup
ENST00000530878.5:c.177+45165_177+45174dup	ENSP00000431586.1:n.177+45165_177+45174dup
NM_001164757.1:c.177+45165_177+45174dup	NP_001158229.1:n.177+45165_177+45174dup
NM_014697.2:c.177+45165_177+45174dup	NP_055512.1:n.177+45165_177+45174dup
NM_014697.3:c.177+45165_177+45174dup MANE Select	NP_055512.1:n.177+45165_177+45174dup
NM_001164757.2:c.177+45165_177+45174dup	NP_001158229.1:n.177+45165_177+45174dup