Canonical Allele Identifier: CA244253450

Gene: NOS1

Linked Data

• dbSNP Id: rs138051850

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.117342413dup , CM000674.2:g.117342413dup	GRCh38
NC_000012.11:g.117780218dup , CM000674.1:g.117780218dup	GRCh37
NC_000012.10:g.116264601dup	NCBI36
NG_011991.2:g.24367dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000317775.11:c.-420-10922dup MANE Select	ENSP00000320758.6:n.-420-10922dup
ENST00000317775.10:c.-420-10922dup	ENSP00000320758.6:n.-420-10922dup
ENST00000549189.1:n.471-10922dup
ENST00000618760.4:c.-420-10922dup	ENSP00000477999.1:n.-420-10922dup
NM_000620.4:c.-420-10922dup	NP_000611.1:n.-420-10922dup
NM_001204218.1:c.-420-10922dup	NP_001191147.1:n.-420-10922dup
XM_011538398.1:c.-420-10922dup	XP_011536700.1:n.-420-10922dup
NM_000620.5:c.-420-10922dup MANE Select	NP_000611.1:n.-420-10922dup
NM_001204218.2:c.-420-10922dup	NP_001191147.1:n.-420-10922dup