Canonical Allele Identifier: CA1144168918
Gene: NOS1AP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.162199385A= , CM000663.2:g.162199385A= GRCh38
NC_000001.10:g.162169175A= , CM000663.1:g.162169175A= GRCh37
NC_000001.9:g.160435799A= NCBI36
NG_015979.1:g.134595A=
NG_015979.2:g.134595A=

Transcript Alleles

HGVS Amino-acid change
ENST00000361897.10:c.177+44909A= MANE Select ENSP00000355133.5:n.177+44909A=
ENST00000361897.9:c.177+44909A= ENSP00000355133.5:n.177+44909A=
ENST00000430120.3:c.177+44909A= ENSP00000396713.3:n.177+44909A=
ENST00000530878.5:c.177+44909A= ENSP00000431586.1:n.177+44909A=
NM_001164757.1:c.177+44909A= NP_001158229.1:n.177+44909A=
NM_014697.2:c.177+44909A= NP_055512.1:n.177+44909A=
NM_014697.3:c.177+44909A= MANE Select NP_055512.1:n.177+44909A=
NM_001164757.2:c.177+44909A= NP_001158229.1:n.177+44909A=