Canonical Allele Identifier: CA1008483619

Gene: NOS1AP

Linked Data

• gnomAD v3: 1-162199649-T-TG
• gnomAD v4: 1-162199649-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162199649_162199650insG , CM000663.2:g.162199649_162199650insG	GRCh38
NC_000001.10:g.162169439_162169440insG , CM000663.1:g.162169439_162169440insG	GRCh37
NC_000001.9:g.160436063_160436064insG	NCBI36
NG_015979.1:g.134859_134860insG
NG_015979.2:g.134859_134860insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361897.10:c.177+45173_177+45174insG MANE Select	ENSP00000355133.5:n.177+45173_177+45174insG
ENST00000361897.9:c.177+45173_177+45174insG	ENSP00000355133.5:n.177+45173_177+45174insG
ENST00000430120.3:c.177+45173_177+45174insG	ENSP00000396713.3:n.177+45173_177+45174insG
ENST00000530878.5:c.177+45173_177+45174insG	ENSP00000431586.1:n.177+45173_177+45174insG
NM_001164757.1:c.177+45173_177+45174insG	NP_001158229.1:n.177+45173_177+45174insG
NM_014697.2:c.177+45173_177+45174insG	NP_055512.1:n.177+45173_177+45174insG
NM_014697.3:c.177+45173_177+45174insG MANE Select	NP_055512.1:n.177+45173_177+45174insG
NM_001164757.2:c.177+45173_177+45174insG	NP_001158229.1:n.177+45173_177+45174insG