Canonical Allele Identifier: CA31618852
Gene: NOS1AP HGNC NCBI

Linked Data

dbSNP Id: rs78315369

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.162115858A>T , CM000663.2:g.162115858A>T GRCh38
NC_000001.10:g.162085648A>T , CM000663.1:g.162085648A>T GRCh37
NC_000001.9:g.160352272A>T NCBI36
NG_015979.1:g.51068A>T
NG_015979.2:g.51068A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000361897.10:c.106-38547A>T MANE Select ENSP00000355133.5:n.106-38547A>T
ENST00000361897.9:c.106-38547A>T ENSP00000355133.5:n.106-38547A>T
ENST00000430120.3:c.106-38547A>T ENSP00000396713.3:n.106-38547A>T
ENST00000530878.5:c.106-38547A>T ENSP00000431586.1:n.106-38547A>T
NM_001164757.1:c.106-38547A>T NP_001158229.1:n.106-38547A>T
NM_014697.2:c.106-38547A>T NP_055512.1:n.106-38547A>T
XR_922217.1:n.884-1956T>A
XR_922219.1:n.713-1956T>A
XR_922221.1:n.713-9110T>A
XR_002958375.1:n.3842-1956T>A
XR_002958378.1:n.3671-1956T>A
NM_014697.3:c.106-38547A>T MANE Select NP_055512.1:n.106-38547A>T
NM_001164757.2:c.106-38547A>T NP_001158229.1:n.106-38547A>T