Canonical Allele Identifier: CA2066036268

Gene: NOS1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.117342155_117342160delinsATCTTT , CM000674.2:g.117342155_117342160delinsATCTTT	GRCh38
NC_000012.11:g.117779960_117779965delinsATCTTT , CM000674.1:g.117779960_117779965delinsATCTTT	GRCh37
NC_000012.10:g.116264343_116264348delinsATCTTT	NCBI36
NG_011991.2:g.24618_24623delinsAAAGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317775.11:c.-420-10671_-420-10666delinsAAAGAT MANE Select	ENSP00000320758.6:n.-420-10671_-420-10666delinsAAAGAT
ENST00000317775.10:c.-420-10671_-420-10666delinsAAAGAT	ENSP00000320758.6:n.-420-10671_-420-10666delinsAAAGAT
ENST00000549189.1:n.471-10671_471-10666delinsAAAGAT
ENST00000618760.4:c.-420-10671_-420-10666delinsAAAGAT	ENSP00000477999.1:n.-420-10671_-420-10666delinsAAAGAT
NM_000620.4:c.-420-10671_-420-10666delinsAAAGAT	NP_000611.1:n.-420-10671_-420-10666delinsAAAGAT
NM_001204218.1:c.-420-10671_-420-10666delinsAAAGAT	NP_001191147.1:n.-420-10671_-420-10666delinsAAAGAT
XM_011538398.1:c.-420-10671_-420-10666delinsAAAGAT	XP_011536700.1:n.-420-10671_-420-10666delinsAAAGAT
NM_000620.5:c.-420-10671_-420-10666delinsAAAGAT MANE Select	NP_000611.1:n.-420-10671_-420-10666delinsAAAGAT
NM_001204218.2:c.-420-10671_-420-10666delinsAAAGAT	NP_001191147.1:n.-420-10671_-420-10666delinsAAAGAT