Canonical Allele Identifier: CA1203016869

Gene: NOS1AP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162115388A= , CM000663.2:g.162115388A=	GRCh38
NC_000001.10:g.162085178A= , CM000663.1:g.162085178A=	GRCh37
NC_000001.9:g.160351802A=	NCBI36
NG_015979.1:g.50598A=
NG_015979.2:g.50598A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361897.10:c.106-39017A= MANE Select	ENSP00000355133.5:n.106-39017A=
ENST00000361897.9:c.106-39017A=	ENSP00000355133.5:n.106-39017A=
ENST00000430120.3:c.106-39017A=	ENSP00000396713.3:n.106-39017A=
ENST00000530878.5:c.106-39017A=	ENSP00000431586.1:n.106-39017A=
NM_001164757.1:c.106-39017A=	NP_001158229.1:n.106-39017A=
NM_014697.2:c.106-39017A=	NP_055512.1:n.106-39017A=
XR_922217.1:n.884-1486T=
XR_922219.1:n.713-1486T=
XR_922221.1:n.713-8640T=
XR_002958375.1:n.3842-1486T=
XR_002958378.1:n.3671-1486T=
NM_014697.3:c.106-39017A= MANE Select	NP_055512.1:n.106-39017A=
NM_001164757.2:c.106-39017A=	NP_001158229.1:n.106-39017A=