Canonical Allele Identifier: CA607677666

Gene: NOS1

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.117323735A>T , CM000674.2:g.117323735A>T	GRCh38
NC_000012.11:g.117761540A>T , CM000674.1:g.117761540A>T	GRCh37
NC_000012.10:g.116245923A>T	NCBI36
NG_011991.2:g.43043T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317775.11:c.725+6610T>A MANE Select	ENSP00000320758.6:n.725+6610T>A
ENST00000317775.10:c.725+6610T>A	ENSP00000320758.6:n.725+6610T>A
ENST00000338101.8:c.725+6610T>A	ENSP00000337459.4:n.725+6610T>A
ENST00000344089.4:c.722+6610T>A	ENSP00000339862.4:n.722+6610T>A
ENST00000618760.4:c.725+6610T>A	ENSP00000477999.1:n.725+6610T>A
NM_000620.4:c.725+6610T>A	NP_000611.1:n.725+6610T>A
NM_001204218.1:c.725+6610T>A	NP_001191147.1:n.725+6610T>A
XM_011538398.1:c.725+6610T>A	XP_011536700.1:n.725+6610T>A
NM_000620.5:c.725+6610T>A MANE Select	NP_000611.1:n.725+6610T>A
NM_001204218.2:c.725+6610T>A	NP_001191147.1:n.725+6610T>A