Canonical Allele Identifier: CA1141549336
Gene: NOS1AP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.162115723C= , CM000663.2:g.162115723C= GRCh38
NC_000001.10:g.162085513C= , CM000663.1:g.162085513C= GRCh37
NC_000001.9:g.160352137C= NCBI36
NG_015979.1:g.50933C=
NG_015979.2:g.50933C=

Transcript Alleles

HGVS Amino-acid change
ENST00000361897.10:c.106-38682C= MANE Select ENSP00000355133.5:n.106-38682C=
ENST00000361897.9:c.106-38682C= ENSP00000355133.5:n.106-38682C=
ENST00000430120.3:c.106-38682C= ENSP00000396713.3:n.106-38682C=
ENST00000530878.5:c.106-38682C= ENSP00000431586.1:n.106-38682C=
NM_001164757.1:c.106-38682C= NP_001158229.1:n.106-38682C=
NM_014697.2:c.106-38682C= NP_055512.1:n.106-38682C=
XR_922217.1:n.884-1821G=
XR_922219.1:n.713-1821G=
XR_922221.1:n.713-8975G=
XR_002958375.1:n.3842-1821G=
XR_002958378.1:n.3671-1821G=
NM_014697.3:c.106-38682C= MANE Select NP_055512.1:n.106-38682C=
NM_001164757.2:c.106-38682C= NP_001158229.1:n.106-38682C=