Canonical Allele Identifier: CA2254020867

Gene: NOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27797598_27797599delinsCT , CM000679.2:g.27797598_27797599delinsCT	GRCh38
NC_000017.10:g.26124624_26124625delinsCT , CM000679.1:g.26124624_26124625delinsCT	GRCh37
NC_000017.9:g.23148751_23148752delinsCT	NCBI36
NG_011470.1:g.7931_7932delinsAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000697337.1:c.110+1101_110+1102delinsAG	ENSP00000513259.1:n.110+1101_110+1102deli...
ENST00000313735.11:c.110+1101_110+1102delinsAG MANE Select	ENSP00000327251.6:n.110+1101_110+1102deli...
ENST00000313735.10:c.110+1101_110+1102delinsAG	ENSP00000327251.6:n.110+1101_110+1102deli...
ENST00000621962.1:c.110+1101_110+1102delinsAG	ENSP00000482291.1:n.110+1101_110+1102deli...
NM_000625.4:c.110+1101_110+1102delinsAG MANE Select	NP_000616.3:n.110+1101_110+1102delinsAG
XM_011524859.1:c.110+1101_110+1102delinsAG	XP_011523161.1:n.110+1101_110+1102delinsA...
XM_011524861.1:c.110+1101_110+1102delinsAG	XP_011523163.1:n.110+1101_110+1102delinsA...