Canonical Allele Identifier: CA1203016987

Gene: NOS1AP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162115695_162115698delinsGGGA , CM000663.2:g.162115695_162115698delinsGGGA	GRCh38
NC_000001.10:g.162085485_162085488delinsGGGA , CM000663.1:g.162085485_162085488delinsGGGA	GRCh37
NC_000001.9:g.160352109_160352112delinsGGGA	NCBI36
NG_015979.1:g.50905_50908delinsGGGA
NG_015979.2:g.50905_50908delinsGGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361897.10:c.106-38710_106-38707delinsGGGA MANE Select	ENSP00000355133.5:n.106-38710_106-38707delinsGGGA
ENST00000361897.9:c.106-38710_106-38707delinsGGGA	ENSP00000355133.5:n.106-38710_106-38707delinsGGGA
ENST00000430120.3:c.106-38710_106-38707delinsGGGA	ENSP00000396713.3:n.106-38710_106-38707delinsGGGA
ENST00000530878.5:c.106-38710_106-38707delinsGGGA	ENSP00000431586.1:n.106-38710_106-38707delinsGGGA
NM_001164757.1:c.106-38710_106-38707delinsGGGA	NP_001158229.1:n.106-38710_106-38707delinsGGGA
NM_014697.2:c.106-38710_106-38707delinsGGGA	NP_055512.1:n.106-38710_106-38707delinsGGGA
XR_922217.1:n.884-1796_884-1793delinsTCCC
XR_922219.1:n.713-1796_713-1793delinsTCCC
XR_922221.1:n.713-8950_713-8947delinsTCCC
XR_002958375.1:n.3842-1796_3842-1793delinsTCCC
XR_002958378.1:n.3671-1796_3671-1793delinsTCCC
NM_014697.3:c.106-38710_106-38707delinsGGGA MANE Select	NP_055512.1:n.106-38710_106-38707delinsGGGA
NM_001164757.2:c.106-38710_106-38707delinsGGGA	NP_001158229.1:n.106-38710_106-38707delinsGGGA