Canonical Allele Identifier: CA1203016905

Gene: NOS1AP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162115461_162115464delinsAGTT , CM000663.2:g.162115461_162115464delinsAGTT	GRCh38
NC_000001.10:g.162085251_162085254delinsAGTT , CM000663.1:g.162085251_162085254delinsAGTT	GRCh37
NC_000001.9:g.160351875_160351878delinsAGTT	NCBI36
NG_015979.1:g.50671_50674delinsAGTT
NG_015979.2:g.50671_50674delinsAGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361897.10:c.106-38944_106-38941delinsAGTT MANE Select	ENSP00000355133.5:n.106-38944_106-38941delinsAGTT
ENST00000361897.9:c.106-38944_106-38941delinsAGTT	ENSP00000355133.5:n.106-38944_106-38941delinsAGTT
ENST00000430120.3:c.106-38944_106-38941delinsAGTT	ENSP00000396713.3:n.106-38944_106-38941delinsAGTT
ENST00000530878.5:c.106-38944_106-38941delinsAGTT	ENSP00000431586.1:n.106-38944_106-38941delinsAGTT
NM_001164757.1:c.106-38944_106-38941delinsAGTT	NP_001158229.1:n.106-38944_106-38941delinsAGTT
NM_014697.2:c.106-38944_106-38941delinsAGTT	NP_055512.1:n.106-38944_106-38941delinsAGTT
XR_922217.1:n.884-1562_884-1559delinsAACT
XR_922219.1:n.713-1562_713-1559delinsAACT
XR_922221.1:n.713-8716_713-8713delinsAACT
XR_002958375.1:n.3842-1562_3842-1559delinsAACT
XR_002958378.1:n.3671-1562_3671-1559delinsAACT
NM_014697.3:c.106-38944_106-38941delinsAGTT MANE Select	NP_055512.1:n.106-38944_106-38941delinsAGTT
NM_001164757.2:c.106-38944_106-38941delinsAGTT	NP_001158229.1:n.106-38944_106-38941delinsAGTT