Canonical Allele Identifier: CA1203016852

Gene: NOS1AP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162115329_162115330delinsCA , CM000663.2:g.162115329_162115330delinsCA	GRCh38
NC_000001.10:g.162085119_162085120delinsCA , CM000663.1:g.162085119_162085120delinsCA	GRCh37
NC_000001.9:g.160351743_160351744delinsCA	NCBI36
NG_015979.1:g.50539_50540delinsCA
NG_015979.2:g.50539_50540delinsCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000361897.10:c.106-39076_106-39075delinsCA MANE Select	ENSP00000355133.5:n.106-39076_106-39075delinsCA
ENST00000361897.9:c.106-39076_106-39075delinsCA	ENSP00000355133.5:n.106-39076_106-39075delinsCA
ENST00000430120.3:c.106-39076_106-39075delinsCA	ENSP00000396713.3:n.106-39076_106-39075delinsCA
ENST00000530878.5:c.106-39076_106-39075delinsCA	ENSP00000431586.1:n.106-39076_106-39075delinsCA
NM_001164757.1:c.106-39076_106-39075delinsCA	NP_001158229.1:n.106-39076_106-39075delinsCA
NM_014697.2:c.106-39076_106-39075delinsCA	NP_055512.1:n.106-39076_106-39075delinsCA
XR_922217.1:n.884-1428_884-1427delinsTG
XR_922219.1:n.713-1428_713-1427delinsTG
XR_922221.1:n.713-8582_713-8581delinsTG
XR_002958375.1:n.3842-1428_3842-1427delinsTG
XR_002958378.1:n.3671-1428_3671-1427delinsTG
NM_014697.3:c.106-39076_106-39075delinsCA MANE Select	NP_055512.1:n.106-39076_106-39075delinsCA
NM_001164757.2:c.106-39076_106-39075delinsCA	NP_001158229.1:n.106-39076_106-39075delinsCA