Canonical Allele Identifier: CA890271259

Gene: NOS1AP

Linked Data

• dbSNP Id: rs1265893571
• gnomAD v3: 1-162254754-T-C
• gnomAD v4: 1-162254754-T-C
• MyVariant Identifiers: chr1:g.162224544T>C (hg19) ; chr1:g.162254754T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162254754T>C , CM000663.2:g.162254754T>C	GRCh38
NC_000001.10:g.162224544T>C , CM000663.1:g.162224544T>C	GRCh37
NC_000001.9:g.160491168T>C	NCBI36
NG_015979.1:g.189964T>C
NG_015979.2:g.189964T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000361897.10:c.178-32590T>C MANE Select	ENSP00000355133.5:n.178-32590T>C
ENST00000361897.9:c.178-32590T>C	ENSP00000355133.5:n.178-32590T>C
ENST00000430120.3:c.178-32590T>C	ENSP00000396713.3:n.178-32590T>C
ENST00000530878.5:c.178-32590T>C	ENSP00000431586.1:n.178-32590T>C
NM_001164757.1:c.178-32590T>C	NP_001158229.1:n.178-32590T>C
NM_014697.2:c.178-32590T>C	NP_055512.1:n.178-32590T>C
NM_014697.3:c.178-32590T>C MANE Select	NP_055512.1:n.178-32590T>C
NM_001164757.2:c.178-32590T>C	NP_001158229.1:n.178-32590T>C