Canonical Allele Identifier: CA1203016902

Gene: NOS1AP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162115457_162115458delinsTG , CM000663.2:g.162115457_162115458delinsTG	GRCh38
NC_000001.10:g.162085247_162085248delinsTG , CM000663.1:g.162085247_162085248delinsTG	GRCh37
NC_000001.9:g.160351871_160351872delinsTG	NCBI36
NG_015979.1:g.50667_50668delinsTG
NG_015979.2:g.50667_50668delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361897.10:c.106-38948_106-38947delinsTG MANE Select	ENSP00000355133.5:n.106-38948_106-38947delinsTG
ENST00000361897.9:c.106-38948_106-38947delinsTG	ENSP00000355133.5:n.106-38948_106-38947delinsTG
ENST00000430120.3:c.106-38948_106-38947delinsTG	ENSP00000396713.3:n.106-38948_106-38947delinsTG
ENST00000530878.5:c.106-38948_106-38947delinsTG	ENSP00000431586.1:n.106-38948_106-38947delinsTG
NM_001164757.1:c.106-38948_106-38947delinsTG	NP_001158229.1:n.106-38948_106-38947delinsTG
NM_014697.2:c.106-38948_106-38947delinsTG	NP_055512.1:n.106-38948_106-38947delinsTG
XR_922217.1:n.884-1556_884-1555delinsCA
XR_922219.1:n.713-1556_713-1555delinsCA
XR_922221.1:n.713-8710_713-8709delinsCA
XR_002958375.1:n.3842-1556_3842-1555delinsCA
XR_002958378.1:n.3671-1556_3671-1555delinsCA
NM_014697.3:c.106-38948_106-38947delinsTG MANE Select	NP_055512.1:n.106-38948_106-38947delinsTG
NM_001164757.2:c.106-38948_106-38947delinsTG	NP_001158229.1:n.106-38948_106-38947delinsTG