Canonical Allele Identifier: CA2697428784

Gene: NOS1AP

Linked Data

• dbSNP Id: rs2102045656

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162116003_162116034del , CM000663.2:g.162116003_162116034del	GRCh38
NC_000001.10:g.162085793_162085824del , CM000663.1:g.162085793_162085824del	GRCh37
NC_000001.9:g.160352417_160352448del	NCBI36
NG_015979.1:g.51213_51244del
NG_015979.2:g.51213_51244del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361897.10:c.106-38402_106-38371del MANE Select	ENSP00000355133.5:n.106-38402_106-38371del
ENST00000361897.9:c.106-38402_106-38371del	ENSP00000355133.5:n.106-38402_106-38371del
ENST00000430120.3:c.106-38402_106-38371del	ENSP00000396713.3:n.106-38402_106-38371del
ENST00000530878.5:c.106-38402_106-38371del	ENSP00000431586.1:n.106-38402_106-38371del
NM_001164757.1:c.106-38402_106-38371del	NP_001158229.1:n.106-38402_106-38371del
NM_014697.2:c.106-38402_106-38371del	NP_055512.1:n.106-38402_106-38371del
XR_922217.1:n.884-2116_884-2085del
XR_922219.1:n.713-2116_713-2085del
XR_922221.1:n.713-9270_713-9239del
XR_002958375.1:n.3842-2116_3842-2085del
XR_002958378.1:n.3671-2116_3671-2085del
NM_014697.3:c.106-38402_106-38371del MANE Select	NP_055512.1:n.106-38402_106-38371del
NM_001164757.2:c.106-38402_106-38371del	NP_001158229.1:n.106-38402_106-38371del