Canonical Allele Identifier: CA2685610431

Gene: NOS3

Linked Data

• gnomAD v4: 7-151001483-TGGG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151001485_151001487del , CM000669.2:g.151001485_151001487del	GRCh38
NC_000007.13:g.150698573_150698575del , CM000669.1:g.150698573_150698575del	GRCh37
NC_000007.12:g.150329506_150329508del	NCBI36
NG_011992.1:g.15427_15429del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297494.8:c.1429-59_1429-57del MANE Select	ENSP00000297494.3:n.1429-59_1429-57del
ENST00000297494.7:c.1429-59_1429-57del	ENSP00000297494.3:n.1429-59_1429-57del
ENST00000461406.5:c.811-59_811-57del	ENSP00000417143.1:n.811-59_811-57del
ENST00000467517.1:c.1429-59_1429-57del	ENSP00000420551.1:n.1429-59_1429-57del
ENST00000484524.5:c.1429-59_1429-57del	ENSP00000420215.1:n.1429-59_1429-57del
NM_000603.4:c.1429-59_1429-57del	NP_000594.2:n.1429-59_1429-57del
NM_001160109.1:c.1429-59_1429-57del	NP_001153581.1:n.1429-59_1429-57del
NM_001160110.1:c.1429-59_1429-57del	NP_001153582.1:n.1429-59_1429-57del
NM_001160111.1:c.1429-59_1429-57del	NP_001153583.1:n.1429-59_1429-57del
XM_006716002.2:c.1429-59_1429-57del	XP_006716065.1:n.1429-59_1429-57del
NM_000603.5:c.1429-59_1429-57del MANE Select	NP_000594.2:n.1429-59_1429-57del
NM_001160109.2:c.1429-59_1429-57del	NP_001153581.1:n.1429-59_1429-57del