Canonical Allele Identifier: CA1203049795
Gene: NOS1AP HGNC NCBI

Linked Data

dbSNP Id: rs1651914817

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.162199493_162199499dup , CM000663.2:g.162199493_162199499dup GRCh38
NC_000001.10:g.162169283_162169289dup , CM000663.1:g.162169283_162169289dup GRCh37
NC_000001.9:g.160435907_160435913dup NCBI36
NG_015979.1:g.134703_134709dup
NG_015979.2:g.134703_134709dup

Transcript Alleles

HGVS Amino-acid change
ENST00000361897.10:c.177+45017_177+45023dup MANE Select ENSP00000355133.5:n.177+45017_177+45023du...
ENST00000361897.9:c.177+45017_177+45023dup ENSP00000355133.5:n.177+45017_177+45023du...
ENST00000430120.3:c.177+45017_177+45023dup ENSP00000396713.3:n.177+45017_177+45023du...
ENST00000530878.5:c.177+45017_177+45023dup ENSP00000431586.1:n.177+45017_177+45023du...
NM_001164757.1:c.177+45017_177+45023dup NP_001158229.1:n.177+45017_177+45023dup
NM_014697.2:c.177+45017_177+45023dup NP_055512.1:n.177+45017_177+45023dup
NM_014697.3:c.177+45017_177+45023dup MANE Select NP_055512.1:n.177+45017_177+45023dup
NM_001164757.2:c.177+45017_177+45023dup NP_001158229.1:n.177+45017_177+45023dup