Canonical Allele Identifier: CA2621193438

Gene: NOS1

Linked Data

• gnomAD v4: 12-117214974-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.117214974G>T , CM000674.2:g.117214974G>T	GRCh38
NC_000012.11:g.117652779G>T , CM000674.1:g.117652779G>T	GRCh37
NC_000012.10:g.116137162G>T	NCBI36
NG_011991.2:g.151804C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000317775.11:c.*335C>A MANE Select	ENSP00000320758.6:n.*335C>A
ENST00000317775.10:c.*335C>A	ENSP00000320758.6:n.*335C>A
ENST00000618760.4:c.*335C>A	ENSP00000477999.1:n.*335C>A
NM_000620.4:c.*335C>A	NP_000611.1:n.*335C>A
NM_001204213.1:c.*335C>A	NP_001191142.1:n.*335C>A
NM_001204214.1:c.*335C>A	NP_001191143.1:n.*335C>A
NM_001204218.1:c.*335C>A	NP_001191147.1:n.*335C>A
XM_011538398.1:c.*335C>A	XP_011536700.1:n.*335C>A
NM_000620.5:c.*335C>A MANE Select	NP_000611.1:n.*335C>A
NM_001204213.2:c.*335C>A	NP_001191142.1:n.*335C>A
NM_001204214.2:c.*335C>A	NP_001191143.1:n.*335C>A
NM_001204218.2:c.*335C>A	NP_001191147.1:n.*335C>A