Canonical Allele Identifier: CA1203049782

Gene: NOS1AP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162199460_162199461delinsTA , CM000663.2:g.162199460_162199461delinsTA	GRCh38
NC_000001.10:g.162169250_162169251delinsTA , CM000663.1:g.162169250_162169251delinsTA	GRCh37
NC_000001.9:g.160435874_160435875delinsTA	NCBI36
NG_015979.1:g.134670_134671delinsTA
NG_015979.2:g.134670_134671delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361897.10:c.177+44984_177+44985delinsTA MANE Select	ENSP00000355133.5:n.177+44984_177+44985delinsTA
ENST00000361897.9:c.177+44984_177+44985delinsTA	ENSP00000355133.5:n.177+44984_177+44985delinsTA
ENST00000430120.3:c.177+44984_177+44985delinsTA	ENSP00000396713.3:n.177+44984_177+44985delinsTA
ENST00000530878.5:c.177+44984_177+44985delinsTA	ENSP00000431586.1:n.177+44984_177+44985delinsTA
NM_001164757.1:c.177+44984_177+44985delinsTA	NP_001158229.1:n.177+44984_177+44985delinsTA
NM_014697.2:c.177+44984_177+44985delinsTA	NP_055512.1:n.177+44984_177+44985delinsTA
NM_014697.3:c.177+44984_177+44985delinsTA MANE Select	NP_055512.1:n.177+44984_177+44985delinsTA
NM_001164757.2:c.177+44984_177+44985delinsTA	NP_001158229.1:n.177+44984_177+44985delinsTA