Canonical Allele Identifier: CA2066036528

Gene: NOS1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.117342354_117342355delinsCA , CM000674.2:g.117342354_117342355delinsCA	GRCh38
NC_000012.11:g.117780159_117780160delinsCA , CM000674.1:g.117780159_117780160delinsCA	GRCh37
NC_000012.10:g.116264542_116264543delinsCA	NCBI36
NG_011991.2:g.24423_24424delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317775.11:c.-420-10866_-420-10865delinsTG MANE Select	ENSP00000320758.6:n.-420-10866_-420-10865delinsTG
ENST00000317775.10:c.-420-10866_-420-10865delinsTG	ENSP00000320758.6:n.-420-10866_-420-10865delinsTG
ENST00000549189.1:n.471-10866_471-10865delinsTG
ENST00000618760.4:c.-420-10866_-420-10865delinsTG	ENSP00000477999.1:n.-420-10866_-420-10865delinsTG
NM_000620.4:c.-420-10866_-420-10865delinsTG	NP_000611.1:n.-420-10866_-420-10865delinsTG
NM_001204218.1:c.-420-10866_-420-10865delinsTG	NP_001191147.1:n.-420-10866_-420-10865delinsTG
XM_011538398.1:c.-420-10866_-420-10865delinsTG	XP_011536700.1:n.-420-10866_-420-10865delinsTG
NM_000620.5:c.-420-10866_-420-10865delinsTG MANE Select	NP_000611.1:n.-420-10866_-420-10865delinsTG
NM_001204218.2:c.-420-10866_-420-10865delinsTG	NP_001191147.1:n.-420-10866_-420-10865delinsTG