Canonical Allele Identifier: CA2066032782
Gene: NOS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117339391_117339393delinsCTG , CM000674.2:g.117339391_117339393delinsCTG GRCh38
NC_000012.11:g.117777196_117777198delinsCTG , CM000674.1:g.117777196_117777198delinsCTG GRCh37
NC_000012.10:g.116261579_116261581delinsCTG NCBI36
NG_011991.2:g.27385_27387delinsCAG

Transcript Alleles

HGVS Amino-acid change
ENST00000317775.11:c.-420-7904_-420-7902delinsCAG MANE Select ENSP00000320758.6:n.-420-7904_-420-7902de...
ENST00000317775.10:c.-420-7904_-420-7902delinsCAG ENSP00000320758.6:n.-420-7904_-420-7902de...
ENST00000549189.1:n.471-7904_471-7902delinsCAG
ENST00000618760.4:c.-420-7904_-420-7902delinsCAG ENSP00000477999.1:n.-420-7904_-420-7902de...
NM_000620.4:c.-420-7904_-420-7902delinsCAG NP_000611.1:n.-420-7904_-420-7902delinsCA...
NM_001204218.1:c.-420-7904_-420-7902delinsCAG NP_001191147.1:n.-420-7904_-420-7902delin...
XM_011538398.1:c.-420-7904_-420-7902delinsCAG XP_011536700.1:n.-420-7904_-420-7902delin...
NM_000620.5:c.-420-7904_-420-7902delinsCAG MANE Select NP_000611.1:n.-420-7904_-420-7902delinsCA...
NM_001204218.2:c.-420-7904_-420-7902delinsCAG NP_001191147.1:n.-420-7904_-420-7902delin...
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