Canonical Allele Identifier: CA890261968

Gene: NOS1AP

Linked Data

• dbSNP Id: rs1395974702
• MyVariant Identifiers: chr1:g.162085248del (hg19) ; chr1:g.162115458del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162115460del , CM000663.2:g.162115460del	GRCh38
NC_000001.10:g.162085250del , CM000663.1:g.162085250del	GRCh37
NC_000001.9:g.160351874del	NCBI36
NG_015979.1:g.50670del
NG_015979.2:g.50670del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361897.10:c.106-38945del MANE Select	ENSP00000355133.5:n.106-38945del
ENST00000361897.9:c.106-38945del	ENSP00000355133.5:n.106-38945del
ENST00000430120.3:c.106-38945del	ENSP00000396713.3:n.106-38945del
ENST00000530878.5:c.106-38945del	ENSP00000431586.1:n.106-38945del
NM_001164757.1:c.106-38945del	NP_001158229.1:n.106-38945del
NM_014697.2:c.106-38945del	NP_055512.1:n.106-38945del
XR_922217.1:n.884-1556del
XR_922219.1:n.713-1556del
XR_922221.1:n.713-8710del
XR_002958375.1:n.3842-1556del
XR_002958378.1:n.3671-1556del
NM_014697.3:c.106-38945del MANE Select	NP_055512.1:n.106-38945del
NM_001164757.2:c.106-38945del	NP_001158229.1:n.106-38945del