Canonical Allele Identifier: CA2066054732
Gene: NOS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117357939G= , CM000674.2:g.117357939G= GRCh38
NC_000012.11:g.117795744G= , CM000674.1:g.117795744G= GRCh37
NC_000012.10:g.116280127G= NCBI36
NG_011991.2:g.8839C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000317775.11:c.-421+3573C= MANE Select ENSP00000320758.6:n.-421+3573C=
ENST00000317775.10:c.-421+3573C= ENSP00000320758.6:n.-421+3573C=
ENST00000477584.1:n.118+3573C=
ENST00000549189.1:n.471-26450C=
ENST00000618760.4:c.-421+3573C= ENSP00000477999.1:n.-421+3573C=
NM_000620.4:c.-421+3573C= NP_000611.1:n.-421+3573C=
NM_001204218.1:c.-421+3573C= NP_001191147.1:n.-421+3573C=
XM_011538398.1:c.-421+1052C= XP_011536700.1:n.-421+1052C=
NM_000620.5:c.-421+3573C= MANE Select NP_000611.1:n.-421+3573C=
NM_001204218.2:c.-421+3573C= NP_001191147.1:n.-421+3573C=
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