Canonical Allele Identifier: CA2066036266

Gene: NOS1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.117342154_117342159delinsCATCTT , CM000674.2:g.117342154_117342159delinsCATCTT	GRCh38
NC_000012.11:g.117779959_117779964delinsCATCTT , CM000674.1:g.117779959_117779964delinsCATCTT	GRCh37
NC_000012.10:g.116264342_116264347delinsCATCTT	NCBI36
NG_011991.2:g.24619_24624delinsAAGATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317775.11:c.-420-10670_-420-10665delinsAAGATG MANE Select	ENSP00000320758.6:n.-420-10670_-420-10665delinsAAGATG
ENST00000317775.10:c.-420-10670_-420-10665delinsAAGATG	ENSP00000320758.6:n.-420-10670_-420-10665delinsAAGATG
ENST00000549189.1:n.471-10670_471-10665delinsAAGATG
ENST00000618760.4:c.-420-10670_-420-10665delinsAAGATG	ENSP00000477999.1:n.-420-10670_-420-10665delinsAAGATG
NM_000620.4:c.-420-10670_-420-10665delinsAAGATG	NP_000611.1:n.-420-10670_-420-10665delinsAAGATG
NM_001204218.1:c.-420-10670_-420-10665delinsAAGATG	NP_001191147.1:n.-420-10670_-420-10665delinsAAGATG
XM_011538398.1:c.-420-10670_-420-10665delinsAAGATG	XP_011536700.1:n.-420-10670_-420-10665delinsAAGATG
NM_000620.5:c.-420-10670_-420-10665delinsAAGATG MANE Select	NP_000611.1:n.-420-10670_-420-10665delinsAAGATG
NM_001204218.2:c.-420-10670_-420-10665delinsAAGATG	NP_001191147.1:n.-420-10670_-420-10665delinsAAGATG