Canonical Allele Identifier: CA1008481782

Gene: NOS1AP

Linked Data

• dbSNP Id: rs1653978659
• gnomAD v3: 1-162254959-T-C
• gnomAD v4: 1-162254959-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162254959T>C , CM000663.2:g.162254959T>C	GRCh38
NC_000001.10:g.162224749T>C , CM000663.1:g.162224749T>C	GRCh37
NC_000001.9:g.160491373T>C	NCBI36
NG_015979.1:g.190169T>C
NG_015979.2:g.190169T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361897.10:c.178-32385T>C MANE Select	ENSP00000355133.5:n.178-32385T>C
ENST00000361897.9:c.178-32385T>C	ENSP00000355133.5:n.178-32385T>C
ENST00000430120.3:c.178-32385T>C	ENSP00000396713.3:n.178-32385T>C
ENST00000530878.5:c.178-32385T>C	ENSP00000431586.1:n.178-32385T>C
NM_001164757.1:c.178-32385T>C	NP_001158229.1:n.178-32385T>C
NM_014697.2:c.178-32385T>C	NP_055512.1:n.178-32385T>C
NM_014697.3:c.178-32385T>C MANE Select	NP_055512.1:n.178-32385T>C
NM_001164757.2:c.178-32385T>C	NP_001158229.1:n.178-32385T>C