Canonical Allele Identifier: CA2065999925

Gene: NOS1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.117307354_117307355delinsCT , CM000674.2:g.117307354_117307355delinsCT	GRCh38
NC_000012.11:g.117745159_117745160delinsCT , CM000674.1:g.117745159_117745160delinsCT	GRCh37
NC_000012.10:g.116229542_116229543delinsCT	NCBI36
NG_011991.2:g.59423_59424delinsAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000317775.11:c.852+4111_852+4112delinsAG MANE Select	ENSP00000320758.6:n.852+4111_852+4112deli...
ENST00000317775.10:c.852+4111_852+4112delinsAG	ENSP00000320758.6:n.852+4111_852+4112deli...
ENST00000338101.8:c.852+4111_852+4112delinsAG	ENSP00000337459.4:n.852+4111_852+4112deli...
ENST00000344089.4:c.849+4111_849+4112delinsAG	ENSP00000339862.4:n.849+4111_849+4112deli...
ENST00000618760.4:c.852+4111_852+4112delinsAG	ENSP00000477999.1:n.852+4111_852+4112deli...
NM_000620.4:c.852+4111_852+4112delinsAG	NP_000611.1:n.852+4111_852+4112delinsAG
NM_001204214.1:c.-213+1962_-213+1963delinsAG	NP_001191143.1:n.-213+1962_-213+1963delin...
NM_001204218.1:c.852+4111_852+4112delinsAG	NP_001191147.1:n.852+4111_852+4112delinsA...
XM_011538398.1:c.852+4111_852+4112delinsAG	XP_011536700.1:n.852+4111_852+4112delinsA...
NM_000620.5:c.852+4111_852+4112delinsAG MANE Select	NP_000611.1:n.852+4111_852+4112delinsAG
NM_001204214.2:c.-213+1962_-213+1963delinsAG	NP_001191143.1:n.-213+1962_-213+1963delin...
NM_001204218.2:c.852+4111_852+4112delinsAG	NP_001191147.1:n.852+4111_852+4112delinsA...