Canonical Allele Identifier: CA1203017072
Gene: NOS1AP HGNC NCBI

Linked Data

dbSNP Id: rs10494366
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.162115895G>C , CM000663.2:g.162115895G>C GRCh38
NC_000001.10:g.162085685G>C , CM000663.1:g.162085685G>C GRCh37
NC_000001.9:g.160352309G>C NCBI36
NG_015979.1:g.51105G>C
NG_015979.2:g.51105G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000361897.10:c.106-38510G>C MANE Select ENSP00000355133.5:n.106-38510G>C
ENST00000361897.9:c.106-38510G>C ENSP00000355133.5:n.106-38510G>C
ENST00000430120.3:c.106-38510G>C ENSP00000396713.3:n.106-38510G>C
ENST00000530878.5:c.106-38510G>C ENSP00000431586.1:n.106-38510G>C
NM_001164757.1:c.106-38510G>C NP_001158229.1:n.106-38510G>C
NM_014697.2:c.106-38510G>C NP_055512.1:n.106-38510G>C
XR_922217.1:n.884-1993C>G
XR_922219.1:n.713-1993C>G
XR_922221.1:n.713-9147C>G
XR_002958375.1:n.3842-1993C>G
XR_002958378.1:n.3671-1993C>G
NM_014697.3:c.106-38510G>C MANE Select NP_055512.1:n.106-38510G>C
NM_001164757.2:c.106-38510G>C NP_001158229.1:n.106-38510G>C
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