Canonical Allele Identifier: CA1140301249

Gene: NOS1AP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162163327G= , CM000663.2:g.162163327G=	GRCh38
NC_000001.10:g.162133117G= , CM000663.1:g.162133117G=	GRCh37
NC_000001.9:g.160399741G=	NCBI36
NG_015979.1:g.98537G=
NG_015979.2:g.98537G=

Transcript Alleles

HGVS	Amino-acid Change
NM_014697.3:c.177+8851G= MANE Select	NP_055512.1:n.177+8851G=
ENST00000361897.10:c.177+8851G= MANE Select	ENSP00000355133.5:n.177+8851G=
NM_001164757.1:c.177+8851G=	NP_001158229.1:n.177+8851G=
NM_001164757.2:c.177+8851G=	NP_001158229.1:n.177+8851G=
NM_014697.2:c.177+8851G=	NP_055512.1:n.177+8851G=
ENST00000361897.9:c.177+8851G=	ENSP00000355133.5:n.177+8851G=
ENST00000430120.3:c.177+8851G=	ENSP00000396713.3:n.177+8851G=
ENST00000530878.5:c.177+8851G=	ENSP00000431586.1:n.177+8851G=
XR_002958374.1:n.3671-3944C=
XR_002958375.1:n.3670+4955C=
XR_002958376.1:n.3671-1102C=
XR_002958378.1:n.3670+4955C=
XR_922216.3:n.6416C=
XR_922217.1:n.712+4955C=
XR_922218.1:n.713-3944C=
XR_922219.1:n.712+4955C=
XR_922220.1:n.713-735C=
XR_922221.1:n.712+4955C=
XR_922222.1:n.713-1102C=