Canonical Allele Identifier: CA2066054844

Gene: NOS1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.117358088A= , CM000674.2:g.117358088A=	GRCh38
NC_000012.11:g.117795893A= , CM000674.1:g.117795893A=	GRCh37
NC_000012.10:g.116280276A=	NCBI36
NG_011991.2:g.8690T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000317775.11:c.-421+3424T= MANE Select	ENSP00000320758.6:n.-421+3424T=
ENST00000317775.10:c.-421+3424T=	ENSP00000320758.6:n.-421+3424T=
ENST00000477584.1:n.118+3424T=
ENST00000549189.1:n.471-26599T=
ENST00000618760.4:c.-421+3424T=	ENSP00000477999.1:n.-421+3424T=
NM_000620.4:c.-421+3424T=	NP_000611.1:n.-421+3424T=
NM_001204218.1:c.-421+3424T=	NP_001191147.1:n.-421+3424T=
XM_011538398.1:c.-421+903T=	XP_011536700.1:n.-421+903T=
NM_000620.5:c.-421+3424T= MANE Select	NP_000611.1:n.-421+3424T=
NM_001204218.2:c.-421+3424T=	NP_001191147.1:n.-421+3424T=