Canonical Allele Identifier: CA1203049770

Gene: NOS1AP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162199441_162199446delinsGTCCTC , CM000663.2:g.162199441_162199446delinsGTCCTC	GRCh38
NC_000001.10:g.162169231_162169236delinsGTCCTC , CM000663.1:g.162169231_162169236delinsGTCCTC	GRCh37
NC_000001.9:g.160435855_160435860delinsGTCCTC	NCBI36
NG_015979.1:g.134651_134656delinsGTCCTC
NG_015979.2:g.134651_134656delinsGTCCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361897.10:c.177+44965_177+44970delinsGTCCTC MANE Select	ENSP00000355133.5:n.177+44965_177+44970delinsGTCCTC
ENST00000361897.9:c.177+44965_177+44970delinsGTCCTC	ENSP00000355133.5:n.177+44965_177+44970delinsGTCCTC
ENST00000430120.3:c.177+44965_177+44970delinsGTCCTC	ENSP00000396713.3:n.177+44965_177+44970delinsGTCCTC
ENST00000530878.5:c.177+44965_177+44970delinsGTCCTC	ENSP00000431586.1:n.177+44965_177+44970delinsGTCCTC
NM_001164757.1:c.177+44965_177+44970delinsGTCCTC	NP_001158229.1:n.177+44965_177+44970delinsGTCCTC
NM_014697.2:c.177+44965_177+44970delinsGTCCTC	NP_055512.1:n.177+44965_177+44970delinsGTCCTC
NM_014697.3:c.177+44965_177+44970delinsGTCCTC MANE Select	NP_055512.1:n.177+44965_177+44970delinsGTCCTC
NM_001164757.2:c.177+44965_177+44970delinsGTCCTC	NP_001158229.1:n.177+44965_177+44970delinsGTCCTC