Canonical Allele Identifier: CA526974407

Gene: NOS1AP

Linked Data

• dbSNP Id: rs1407621130
• gnomAD v2: 1-162085865-CCTTTA-C
• gnomAD v3: 1-162116075-CCTTTA-C
• gnomAD v4: 1-162116075-CCTTTA-C
• MyVariant Identifiers: chr1:g.162085866_162085870del (hg19) ; chr1:g.162116076_162116080del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162116079_162116083del , CM000663.2:g.162116079_162116083del	GRCh38
NC_000001.10:g.162085869_162085873del , CM000663.1:g.162085869_162085873del	GRCh37
NC_000001.9:g.160352493_160352497del	NCBI36
NG_015979.1:g.51289_51293del
NG_015979.2:g.51289_51293del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361897.10:c.106-38326_106-38322del MANE Select	ENSP00000355133.5:n.106-38326_106-38322del
ENST00000361897.9:c.106-38326_106-38322del	ENSP00000355133.5:n.106-38326_106-38322del
ENST00000430120.3:c.106-38326_106-38322del	ENSP00000396713.3:n.106-38326_106-38322del
ENST00000530878.5:c.106-38326_106-38322del	ENSP00000431586.1:n.106-38326_106-38322del
NM_001164757.1:c.106-38326_106-38322del	NP_001158229.1:n.106-38326_106-38322del
NM_014697.2:c.106-38326_106-38322del	NP_055512.1:n.106-38326_106-38322del
XR_922217.1:n.884-2178_884-2174del
XR_922219.1:n.713-2178_713-2174del
XR_922221.1:n.713-9332_713-9328del
XR_002958375.1:n.3842-2178_3842-2174del
XR_002958378.1:n.3671-2178_3671-2174del
NM_014697.3:c.106-38326_106-38322del MANE Select	NP_055512.1:n.106-38326_106-38322del
NM_001164757.2:c.106-38326_106-38322del	NP_001158229.1:n.106-38326_106-38322del