Canonical Allele Identifier: CA369857503

Gene: NOS3

Linked Data

• MyVariant Identifiers: chr7:g.150698920T>G (hg19) ; chr7:g.151001832T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151001832T>G , CM000669.2:g.151001832T>G	GRCh38
NC_000007.13:g.150698920T>G , CM000669.1:g.150698920T>G	GRCh37
NC_000007.12:g.150329853T>G	NCBI36
NG_011992.1:g.15774T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297494.8:c.1514T>G MANE Select	ENSP00000297494.3:p.Ile505Ser
ENST00000297494.7:c.1514T>G	ENSP00000297494.3:p.Ile505Ser
ENST00000461406.5:c.896T>G	ENSP00000417143.1:p.Ile299Ser
ENST00000467517.1:c.1514T>G	ENSP00000420551.1:p.Ile505Ser
ENST00000484524.5:c.1514T>G	ENSP00000420215.1:p.Ile505Ser
NM_000603.4:c.1514T>G	NP_000594.2:p.Ile505Ser
NM_001160109.1:c.1514T>G	NP_001153581.1:p.Ile505Ser
NM_001160110.1:c.1514T>G	NP_001153582.1:p.Ile505Ser
NM_001160111.1:c.1514T>G	NP_001153583.1:p.Ile505Ser
XM_006716002.2:c.1514T>G	XP_006716065.1:p.Ile505Ser
NM_000603.5:c.1514T>G MANE Select	NP_000594.2:p.Ile505Ser
NM_001160109.2:c.1514T>G	NP_001153581.1:p.Ile505Ser