Canonical Allele Identifier: CA1203017141

Gene: NOS1AP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162116075_162116080delinsCCTTTA , CM000663.2:g.162116075_162116080delinsCCTTTA	GRCh38
NC_000001.10:g.162085865_162085870delinsCCTTTA , CM000663.1:g.162085865_162085870delinsCCTTTA	GRCh37
NC_000001.9:g.160352489_160352494delinsCCTTTA	NCBI36
NG_015979.1:g.51285_51290delinsCCTTTA
NG_015979.2:g.51285_51290delinsCCTTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361897.10:c.106-38330_106-38325delinsCCTTTA MANE Select	ENSP00000355133.5:n.106-38330_106-38325delinsCCTTTA
ENST00000361897.9:c.106-38330_106-38325delinsCCTTTA	ENSP00000355133.5:n.106-38330_106-38325delinsCCTTTA
ENST00000430120.3:c.106-38330_106-38325delinsCCTTTA	ENSP00000396713.3:n.106-38330_106-38325delinsCCTTTA
ENST00000530878.5:c.106-38330_106-38325delinsCCTTTA	ENSP00000431586.1:n.106-38330_106-38325delinsCCTTTA
NM_001164757.1:c.106-38330_106-38325delinsCCTTTA	NP_001158229.1:n.106-38330_106-38325delinsCCTTTA
NM_014697.2:c.106-38330_106-38325delinsCCTTTA	NP_055512.1:n.106-38330_106-38325delinsCCTTTA
XR_922217.1:n.884-2178_884-2173delinsTAAAGG
XR_922219.1:n.713-2178_713-2173delinsTAAAGG
XR_922221.1:n.713-9332_713-9327delinsTAAAGG
XR_002958375.1:n.3842-2178_3842-2173delinsTAAAGG
XR_002958378.1:n.3671-2178_3671-2173delinsTAAAGG
NM_014697.3:c.106-38330_106-38325delinsCCTTTA MANE Select	NP_055512.1:n.106-38330_106-38325delinsCCTTTA
NM_001164757.2:c.106-38330_106-38325delinsCCTTTA	NP_001158229.1:n.106-38330_106-38325delinsCCTTTA