Canonical Allele Identifier: CA1752441131

Gene: NOS3

Linked Data

• dbSNP Id: rs1795099790

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151001632_151001659del , CM000669.2:g.151001632_151001659del	GRCh38
NC_000007.13:g.150698720_150698747del , CM000669.1:g.150698720_150698747del	GRCh37
NC_000007.12:g.150329653_150329680del	NCBI36
NG_011992.1:g.15574_15601del

Transcript Alleles

HGVS	Amino-acid change
ENST00000297494.8:c.1502+15_1502+42del MANE Select	ENSP00000297494.3:n.1502+15_1502+42del
ENST00000297494.7:c.1502+15_1502+42del	ENSP00000297494.3:n.1502+15_1502+42del
ENST00000461406.5:c.884+15_884+42del	ENSP00000417143.1:n.884+15_884+42del
ENST00000467517.1:c.1502+15_1502+42del	ENSP00000420551.1:n.1502+15_1502+42del
ENST00000484524.5:c.1502+15_1502+42del	ENSP00000420215.1:n.1502+15_1502+42del
NM_000603.4:c.1502+15_1502+42del	NP_000594.2:n.1502+15_1502+42del
NM_001160109.1:c.1502+15_1502+42del	NP_001153581.1:n.1502+15_1502+42del
NM_001160110.1:c.1502+15_1502+42del	NP_001153582.1:n.1502+15_1502+42del
NM_001160111.1:c.1502+15_1502+42del	NP_001153583.1:n.1502+15_1502+42del
XM_006716002.2:c.1502+15_1502+42del	XP_006716065.1:n.1502+15_1502+42del
NM_000603.5:c.1502+15_1502+42del MANE Select	NP_000594.2:n.1502+15_1502+42del
NM_001160109.2:c.1502+15_1502+42del	NP_001153581.1:n.1502+15_1502+42del