Canonical Allele Identifier: CA2993160244

Gene: NOS1AP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162115920_162115924del , CM000663.2:g.162115920_162115924del	GRCh38
NC_000001.10:g.162085710_162085714del , CM000663.1:g.162085710_162085714del	GRCh37
NC_000001.9:g.160352334_160352338del	NCBI36
NG_015979.1:g.51130_51134del
NG_015979.2:g.51130_51134del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361897.10:c.106-38485_106-38481del MANE Select	ENSP00000355133.5:n.106-38485_106-38481del
ENST00000361897.9:c.106-38485_106-38481del	ENSP00000355133.5:n.106-38485_106-38481del
ENST00000430120.3:c.106-38485_106-38481del	ENSP00000396713.3:n.106-38485_106-38481del
ENST00000530878.5:c.106-38485_106-38481del	ENSP00000431586.1:n.106-38485_106-38481del
NM_001164757.1:c.106-38485_106-38481del	NP_001158229.1:n.106-38485_106-38481del
NM_014697.2:c.106-38485_106-38481del	NP_055512.1:n.106-38485_106-38481del
XR_922217.1:n.884-2020_884-2016del
XR_922219.1:n.713-2020_713-2016del
XR_922221.1:n.713-9174_713-9170del
XR_002958375.1:n.3842-2020_3842-2016del
XR_002958378.1:n.3671-2020_3671-2016del
NM_014697.3:c.106-38485_106-38481del MANE Select	NP_055512.1:n.106-38485_106-38481del
NM_001164757.2:c.106-38485_106-38481del	NP_001158229.1:n.106-38485_106-38481del