Canonical Allele Identifier: CA1203017026
Gene: NOS1AP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.162115782A= , CM000663.2:g.162115782A= GRCh38
NC_000001.10:g.162085572A= , CM000663.1:g.162085572A= GRCh37
NC_000001.9:g.160352196A= NCBI36
NG_015979.1:g.50992A=
NG_015979.2:g.50992A=

Transcript Alleles

HGVS Amino-acid change
ENST00000361897.10:c.106-38623A= MANE Select ENSP00000355133.5:n.106-38623A=
ENST00000361897.9:c.106-38623A= ENSP00000355133.5:n.106-38623A=
ENST00000430120.3:c.106-38623A= ENSP00000396713.3:n.106-38623A=
ENST00000530878.5:c.106-38623A= ENSP00000431586.1:n.106-38623A=
NM_001164757.1:c.106-38623A= NP_001158229.1:n.106-38623A=
NM_014697.2:c.106-38623A= NP_055512.1:n.106-38623A=
XR_922217.1:n.884-1880T=
XR_922219.1:n.713-1880T=
XR_922221.1:n.713-9034T=
XR_002958375.1:n.3842-1880T=
XR_002958378.1:n.3671-1880T=
NM_014697.3:c.106-38623A= MANE Select NP_055512.1:n.106-38623A=
NM_001164757.2:c.106-38623A= NP_001158229.1:n.106-38623A=