Canonical Allele Identifier: CA2066054805
Gene: NOS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117358040_117358041delinsCA , CM000674.2:g.117358040_117358041delinsCA GRCh38
NC_000012.11:g.117795845_117795846delinsCA , CM000674.1:g.117795845_117795846delinsCA GRCh37
NC_000012.10:g.116280228_116280229delinsCA NCBI36
NG_011991.2:g.8737_8738delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000317775.11:c.-421+3471_-421+3472delinsTG MANE Select ENSP00000320758.6:n.-421+3471_-421+3472de...
ENST00000317775.10:c.-421+3471_-421+3472delinsTG ENSP00000320758.6:n.-421+3471_-421+3472de...
ENST00000477584.1:n.118+3471_118+3472delinsTG
ENST00000549189.1:n.471-26552_471-26551delinsTG
ENST00000618760.4:c.-421+3471_-421+3472delinsTG ENSP00000477999.1:n.-421+3471_-421+3472de...
NM_000620.4:c.-421+3471_-421+3472delinsTG NP_000611.1:n.-421+3471_-421+3472delinsTG...
NM_001204218.1:c.-421+3471_-421+3472delinsTG NP_001191147.1:n.-421+3471_-421+3472delin...
XM_011538398.1:c.-421+950_-421+951delinsTG XP_011536700.1:n.-421+950_-421+951delinsT...
NM_000620.5:c.-421+3471_-421+3472delinsTG MANE Select NP_000611.1:n.-421+3471_-421+3472delinsTG...
NM_001204218.2:c.-421+3471_-421+3472delinsTG NP_001191147.1:n.-421+3471_-421+3472delin...