Canonical Allele Identifier: CA1008480737

Gene: NOS1AP

Linked Data

• dbSNP Id: rs1647917181
• gnomAD v3: 1-162115695-GGGA-G
• gnomAD v4: 1-162115695-GGGA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162115698_162115700del , CM000663.2:g.162115698_162115700del	GRCh38
NC_000001.10:g.162085488_162085490del , CM000663.1:g.162085488_162085490del	GRCh37
NC_000001.9:g.160352112_160352114del	NCBI36
NG_015979.1:g.50908_50910del
NG_015979.2:g.50908_50910del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361897.10:c.106-38707_106-38705del MANE Select	ENSP00000355133.5:n.106-38707_106-38705del
ENST00000361897.9:c.106-38707_106-38705del	ENSP00000355133.5:n.106-38707_106-38705del
ENST00000430120.3:c.106-38707_106-38705del	ENSP00000396713.3:n.106-38707_106-38705del
ENST00000530878.5:c.106-38707_106-38705del	ENSP00000431586.1:n.106-38707_106-38705del
NM_001164757.1:c.106-38707_106-38705del	NP_001158229.1:n.106-38707_106-38705del
NM_014697.2:c.106-38707_106-38705del	NP_055512.1:n.106-38707_106-38705del
XR_922217.1:n.884-1796_884-1794del
XR_922219.1:n.713-1796_713-1794del
XR_922221.1:n.713-8950_713-8948del
XR_002958375.1:n.3842-1796_3842-1794del
XR_002958378.1:n.3671-1796_3671-1794del
NM_014697.3:c.106-38707_106-38705del MANE Select	NP_055512.1:n.106-38707_106-38705del
NM_001164757.2:c.106-38707_106-38705del	NP_001158229.1:n.106-38707_106-38705del