Canonical Allele Identifier: CA1752441645
Gene: NOS3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151001813_151001814delinsTC , CM000669.2:g.151001813_151001814delinsTC GRCh38
NC_000007.13:g.150698901_150698902delinsTC , CM000669.1:g.150698901_150698902delinsTC GRCh37
NC_000007.12:g.150329834_150329835delinsTC NCBI36
NG_011992.1:g.15755_15756delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000297494.8:c.1503-8_1503-7delinsTC MANE Select ENSP00000297494.3:n.1503-8_1503-7delinsTC
ENST00000297494.7:c.1503-8_1503-7delinsTC ENSP00000297494.3:n.1503-8_1503-7delinsTC
ENST00000461406.5:c.885-8_885-7delinsTC ENSP00000417143.1:n.885-8_885-7delinsTC
ENST00000467517.1:c.1503-8_1503-7delinsTC ENSP00000420551.1:n.1503-8_1503-7delinsTC
ENST00000484524.5:c.1503-8_1503-7delinsTC ENSP00000420215.1:n.1503-8_1503-7delinsTC
NM_000603.4:c.1503-8_1503-7delinsTC NP_000594.2:n.1503-8_1503-7delinsTC
NM_001160109.1:c.1503-8_1503-7delinsTC NP_001153581.1:n.1503-8_1503-7delinsTC
NM_001160110.1:c.1503-8_1503-7delinsTC NP_001153582.1:n.1503-8_1503-7delinsTC
NM_001160111.1:c.1503-8_1503-7delinsTC NP_001153583.1:n.1503-8_1503-7delinsTC
XM_006716002.2:c.1503-8_1503-7delinsTC XP_006716065.1:n.1503-8_1503-7delinsTC
NM_000603.5:c.1503-8_1503-7delinsTC MANE Select NP_000594.2:n.1503-8_1503-7delinsTC
NM_001160109.2:c.1503-8_1503-7delinsTC NP_001153581.1:n.1503-8_1503-7delinsTC