Canonical Allele Identifier: CA1203016912

Gene: NOS1AP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162115485G= , CM000663.2:g.162115485G=	GRCh38
NC_000001.10:g.162085275G= , CM000663.1:g.162085275G=	GRCh37
NC_000001.9:g.160351899G=	NCBI36
NG_015979.1:g.50695G=
NG_015979.2:g.50695G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361897.10:c.106-38920G= MANE Select	ENSP00000355133.5:n.106-38920G=
ENST00000361897.9:c.106-38920G=	ENSP00000355133.5:n.106-38920G=
ENST00000430120.3:c.106-38920G=	ENSP00000396713.3:n.106-38920G=
ENST00000530878.5:c.106-38920G=	ENSP00000431586.1:n.106-38920G=
NM_001164757.1:c.106-38920G=	NP_001158229.1:n.106-38920G=
NM_014697.2:c.106-38920G=	NP_055512.1:n.106-38920G=
XR_922217.1:n.884-1583C=
XR_922219.1:n.713-1583C=
XR_922221.1:n.713-8737C=
XR_002958375.1:n.3842-1583C=
XR_002958378.1:n.3671-1583C=
NM_014697.3:c.106-38920G= MANE Select	NP_055512.1:n.106-38920G=
NM_001164757.2:c.106-38920G=	NP_001158229.1:n.106-38920G=