Canonical Allele Identifier: CA1203017115

Gene: NOS1AP

Linked Data

• dbSNP Id: rs1647934638

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162116013A>C , CM000663.2:g.162116013A>C	GRCh38
NC_000001.10:g.162085803A>C , CM000663.1:g.162085803A>C	GRCh37
NC_000001.9:g.160352427A>C	NCBI36
NG_015979.1:g.51223A>C
NG_015979.2:g.51223A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000361897.10:c.106-38392A>C MANE Select	ENSP00000355133.5:n.106-38392A>C
ENST00000361897.9:c.106-38392A>C	ENSP00000355133.5:n.106-38392A>C
ENST00000430120.3:c.106-38392A>C	ENSP00000396713.3:n.106-38392A>C
ENST00000530878.5:c.106-38392A>C	ENSP00000431586.1:n.106-38392A>C
NM_001164757.1:c.106-38392A>C	NP_001158229.1:n.106-38392A>C
NM_014697.2:c.106-38392A>C	NP_055512.1:n.106-38392A>C
XR_922217.1:n.884-2111T>G
XR_922219.1:n.713-2111T>G
XR_922221.1:n.713-9265T>G
XR_002958375.1:n.3842-2111T>G
XR_002958378.1:n.3671-2111T>G
NM_014697.3:c.106-38392A>C MANE Select	NP_055512.1:n.106-38392A>C
NM_001164757.2:c.106-38392A>C	NP_001158229.1:n.106-38392A>C