Canonical Allele Identifier: CA2254008319

Gene: NOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27769465_27769466delinsTC , CM000679.2:g.27769465_27769466delinsTC	GRCh38
NC_000017.10:g.26096491_26096492delinsTC , CM000679.1:g.26096491_26096492delinsTC	GRCh37
NC_000017.9:g.23120618_23120619delinsTC	NCBI36
NG_011470.1:g.36064_36065delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697337.1:c.*2595+69_*2595+70delinsGA	ENSP00000513259.1:n.*2595+69_*2595+70delinsGA
ENST00000697338.1:c.1707+69_1707+70delinsGA	ENSP00000513260.1:n.1707+69_1707+70delinsGA
ENST00000697339.1:c.893+69_893+70delinsGA	ENSP00000513261.1:n.893+69_893+70delinsGA
ENST00000697340.1:c.*576+69_*576+70delinsGA	ENSP00000513262.1:n.*576+69_*576+70delinsGA
ENST00000697341.1:n.1829+69_1829+70delinsGA
ENST00000313735.11:c.1859+69_1859+70delinsGA MANE Select	ENSP00000327251.6:n.1859+69_1859+70delinsGA
ENST00000646938.1:c.1856+69_1856+70delinsGA	ENSP00000494870.1:n.1856+69_1856+70delinsGA
ENST00000313735.10:c.1859+69_1859+70delinsGA	ENSP00000327251.6:n.1859+69_1859+70delinsGA
ENST00000621962.1:c.1742+69_1742+70delinsGA	ENSP00000482291.1:n.1742+69_1742+70delinsGA
NM_000625.4:c.1859+69_1859+70delinsGA MANE Select	NP_000616.3:n.1859+69_1859+70delinsGA
XM_011524859.1:c.1859+69_1859+70delinsGA	XP_011523161.1:n.1859+69_1859+70delinsGA
XM_011524860.1:c.1856+69_1856+70delinsGA	XP_011523162.1:n.1856+69_1856+70delinsGA
XM_011524861.1:c.1859+69_1859+70delinsGA	XP_011523163.1:n.1859+69_1859+70delinsGA
XM_011524862.1:c.1193+69_1193+70delinsGA	XP_011523164.1:n.1193+69_1193+70delinsGA