Canonical Allele Identifier: CA890261960

Gene: NOS1AP

Linked Data

• dbSNP Id: rs1387566781
• gnomAD v3: 1-162115329-CA-C
• gnomAD v4: 1-162115329-CA-C
• MyVariant Identifiers: chr1:g.162085120del (hg19) ; chr1:g.162115330del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162115332del , CM000663.2:g.162115332del	GRCh38
NC_000001.10:g.162085122del , CM000663.1:g.162085122del	GRCh37
NC_000001.9:g.160351746del	NCBI36
NG_015979.1:g.50542del
NG_015979.2:g.50542del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361897.10:c.106-39073del MANE Select	ENSP00000355133.5:n.106-39073del
ENST00000361897.9:c.106-39073del	ENSP00000355133.5:n.106-39073del
ENST00000430120.3:c.106-39073del	ENSP00000396713.3:n.106-39073del
ENST00000530878.5:c.106-39073del	ENSP00000431586.1:n.106-39073del
NM_001164757.1:c.106-39073del	NP_001158229.1:n.106-39073del
NM_014697.2:c.106-39073del	NP_055512.1:n.106-39073del
XR_922217.1:n.884-1428del
XR_922219.1:n.713-1428del
XR_922221.1:n.713-8582del
XR_002958375.1:n.3842-1428del
XR_002958378.1:n.3671-1428del
NM_014697.3:c.106-39073del MANE Select	NP_055512.1:n.106-39073del
NM_001164757.2:c.106-39073del	NP_001158229.1:n.106-39073del