Canonical Allele Identifier: CA1752472060

Gene: NOS3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151001442_151001444delinsGCT , CM000669.2:g.151001442_151001444delinsGCT	GRCh38
NC_000007.13:g.150698530_150698532delinsGCT , CM000669.1:g.150698530_150698532delinsGCT	GRCh37
NC_000007.12:g.150329463_150329465delinsGCT	NCBI36
NG_011992.1:g.15384_15386delinsGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297494.8:c.1428+17_1428+19delinsGCT MANE Select	ENSP00000297494.3:n.1428+17_1428+19delinsGCT
ENST00000297494.7:c.1428+17_1428+19delinsGCT	ENSP00000297494.3:n.1428+17_1428+19delinsGCT
ENST00000461406.5:c.810+17_810+19delinsGCT	ENSP00000417143.1:n.810+17_810+19delinsGCT
ENST00000467517.1:c.1428+17_1428+19delinsGCT	ENSP00000420551.1:n.1428+17_1428+19delinsGCT
ENST00000484524.5:c.1428+17_1428+19delinsGCT	ENSP00000420215.1:n.1428+17_1428+19delinsGCT
NM_000603.4:c.1428+17_1428+19delinsGCT	NP_000594.2:n.1428+17_1428+19delinsGCT
NM_001160109.1:c.1428+17_1428+19delinsGCT	NP_001153581.1:n.1428+17_1428+19delinsGCT
NM_001160110.1:c.1428+17_1428+19delinsGCT	NP_001153582.1:n.1428+17_1428+19delinsGCT
NM_001160111.1:c.1428+17_1428+19delinsGCT	NP_001153583.1:n.1428+17_1428+19delinsGCT
XM_006716002.2:c.1428+17_1428+19delinsGCT	XP_006716065.1:n.1428+17_1428+19delinsGCT
NM_000603.5:c.1428+17_1428+19delinsGCT MANE Select	NP_000594.2:n.1428+17_1428+19delinsGCT
NM_001160109.2:c.1428+17_1428+19delinsGCT	NP_001153581.1:n.1428+17_1428+19delinsGCT