Canonical Allele Identifier: CA31618542

Gene: NOS1AP

Linked Data

• dbSNP Id: rs958751995
• gnomAD v3: 1-162115537-T-C
• gnomAD v4: 1-162115537-T-C
• MyVariant Identifiers: chr1:g.162085327T>C (hg19) ; chr1:g.162115537T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162115537T>C , CM000663.2:g.162115537T>C	GRCh38
NC_000001.10:g.162085327T>C , CM000663.1:g.162085327T>C	GRCh37
NC_000001.9:g.160351951T>C	NCBI36
NG_015979.1:g.50747T>C
NG_015979.2:g.50747T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361897.10:c.106-38868T>C MANE Select	ENSP00000355133.5:n.106-38868T>C
ENST00000361897.9:c.106-38868T>C	ENSP00000355133.5:n.106-38868T>C
ENST00000430120.3:c.106-38868T>C	ENSP00000396713.3:n.106-38868T>C
ENST00000530878.5:c.106-38868T>C	ENSP00000431586.1:n.106-38868T>C
NM_001164757.1:c.106-38868T>C	NP_001158229.1:n.106-38868T>C
NM_014697.2:c.106-38868T>C	NP_055512.1:n.106-38868T>C
XR_922217.1:n.884-1635A>G
XR_922219.1:n.713-1635A>G
XR_922221.1:n.713-8789A>G
XR_002958375.1:n.3842-1635A>G
XR_002958378.1:n.3671-1635A>G
NM_014697.3:c.106-38868T>C MANE Select	NP_055512.1:n.106-38868T>C
NM_001164757.2:c.106-38868T>C	NP_001158229.1:n.106-38868T>C