Canonical Allele Identifier: CA2513034909

Gene: NOS1AP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162115428_162115429insAAATTAGCT , CM000663.2:g.162115428_162115429insAAATTAGCT	GRCh38
NC_000001.10:g.162085218_162085219insAAATTAGCT , CM000663.1:g.162085218_162085219insAAATTAGCT	GRCh37
NC_000001.9:g.160351842_160351843insAAATTAGCT	NCBI36
NG_015979.1:g.50638_50639insAAATTAGCT
NG_015979.2:g.50638_50639insAAATTAGCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000361897.10:c.106-38977_106-38976insAAATTAGCT MANE Select	ENSP00000355133.5:n.106-38977_106-38976in...
ENST00000361897.9:c.106-38977_106-38976insAAATTAGCT	ENSP00000355133.5:n.106-38977_106-38976in...
ENST00000430120.3:c.106-38977_106-38976insAAATTAGCT	ENSP00000396713.3:n.106-38977_106-38976in...
ENST00000530878.5:c.106-38977_106-38976insAAATTAGCT	ENSP00000431586.1:n.106-38977_106-38976in...
NM_001164757.1:c.106-38977_106-38976insAAATTAGCT	NP_001158229.1:n.106-38977_106-38976insAA...
NM_014697.2:c.106-38977_106-38976insAAATTAGCT	NP_055512.1:n.106-38977_106-38976insAAATT...
XR_922217.1:n.884-1527_884-1526insAGCTAATTT
XR_922219.1:n.713-1527_713-1526insAGCTAATTT
XR_922221.1:n.713-8681_713-8680insAGCTAATTT
XR_002958375.1:n.3842-1527_3842-1526insAGCTAATTT
XR_002958378.1:n.3671-1527_3671-1526insAGCTAATTT
NM_014697.3:c.106-38977_106-38976insAAATTAGCT MANE Select	NP_055512.1:n.106-38977_106-38976insAAATT...
NM_001164757.2:c.106-38977_106-38976insAAATTAGCT	NP_001158229.1:n.106-38977_106-38976insAA...