Canonical Allele Identifier: CA31618546

Gene: NOS1AP

Linked Data

• dbSNP Id: rs964150809
• gnomAD v3: 1-162115540-C-T
• gnomAD v4: 1-162115540-C-T
• MyVariant Identifiers: chr1:g.162085330C>T (hg19) ; chr1:g.162115540C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162115540C>T , CM000663.2:g.162115540C>T	GRCh38
NC_000001.10:g.162085330C>T , CM000663.1:g.162085330C>T	GRCh37
NC_000001.9:g.160351954C>T	NCBI36
NG_015979.1:g.50750C>T
NG_015979.2:g.50750C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361897.10:c.106-38865C>T MANE Select	ENSP00000355133.5:n.106-38865C>T
ENST00000361897.9:c.106-38865C>T	ENSP00000355133.5:n.106-38865C>T
ENST00000430120.3:c.106-38865C>T	ENSP00000396713.3:n.106-38865C>T
ENST00000530878.5:c.106-38865C>T	ENSP00000431586.1:n.106-38865C>T
NM_001164757.1:c.106-38865C>T	NP_001158229.1:n.106-38865C>T
NM_014697.2:c.106-38865C>T	NP_055512.1:n.106-38865C>T
XR_922217.1:n.884-1638G>A
XR_922219.1:n.713-1638G>A
XR_922221.1:n.713-8792G>A
XR_002958375.1:n.3842-1638G>A
XR_002958378.1:n.3671-1638G>A
NM_014697.3:c.106-38865C>T MANE Select	NP_055512.1:n.106-38865C>T
NM_001164757.2:c.106-38865C>T	NP_001158229.1:n.106-38865C>T