Canonical Allele Identifier: CA2685610908

Gene: NOS3

Linked Data

• gnomAD v4: 7-151001999-AAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151002002_151002003del , CM000669.2:g.151002002_151002003del	GRCh38
NC_000007.13:g.150699090_150699091del , CM000669.1:g.150699090_150699091del	GRCh37
NC_000007.12:g.150330023_150330024del	NCBI36
NG_011992.1:g.15944_15945del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297494.8:c.1647+37_1647+38del MANE Select	ENSP00000297494.3:n.1647+37_1647+38del
ENST00000297494.7:c.1647+37_1647+38del	ENSP00000297494.3:n.1647+37_1647+38del
ENST00000460603.1:n.99+37_99+38del
ENST00000461406.5:c.1029+37_1029+38del	ENSP00000417143.1:n.1029+37_1029+38del
ENST00000467517.1:c.1647+37_1647+38del	ENSP00000420551.1:n.1647+37_1647+38del
ENST00000484524.5:c.1647+37_1647+38del	ENSP00000420215.1:n.1647+37_1647+38del
NM_000603.4:c.1647+37_1647+38del	NP_000594.2:n.1647+37_1647+38del
NM_001160109.1:c.1647+37_1647+38del	NP_001153581.1:n.1647+37_1647+38del
NM_001160110.1:c.1647+37_1647+38del	NP_001153582.1:n.1647+37_1647+38del
NM_001160111.1:c.1647+37_1647+38del	NP_001153583.1:n.1647+37_1647+38del
XM_006716002.2:c.1647+37_1647+38del	XP_006716065.1:n.1647+37_1647+38del
NM_000603.5:c.1647+37_1647+38del MANE Select	NP_000594.2:n.1647+37_1647+38del
NM_001160109.2:c.1647+37_1647+38del	NP_001153581.1:n.1647+37_1647+38del