Canonical Allele Identifier: CA1008483357

Gene: NOS1AP

Linked Data

• dbSNP Id: rs1651911597
• gnomAD v3: 1-162199406-G-C
• gnomAD v4: 1-162199406-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162199406G>C , CM000663.2:g.162199406G>C	GRCh38
NC_000001.10:g.162169196G>C , CM000663.1:g.162169196G>C	GRCh37
NC_000001.9:g.160435820G>C	NCBI36
NG_015979.1:g.134616G>C
NG_015979.2:g.134616G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000361897.10:c.177+44930G>C MANE Select	ENSP00000355133.5:n.177+44930G>C
ENST00000361897.9:c.177+44930G>C	ENSP00000355133.5:n.177+44930G>C
ENST00000430120.3:c.177+44930G>C	ENSP00000396713.3:n.177+44930G>C
ENST00000530878.5:c.177+44930G>C	ENSP00000431586.1:n.177+44930G>C
NM_001164757.1:c.177+44930G>C	NP_001158229.1:n.177+44930G>C
NM_014697.2:c.177+44930G>C	NP_055512.1:n.177+44930G>C
NM_014697.3:c.177+44930G>C MANE Select	NP_055512.1:n.177+44930G>C
NM_001164757.2:c.177+44930G>C	NP_001158229.1:n.177+44930G>C