Canonical Allele Identifier: CA2254006492

Gene: NOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27764946_27764948delinsTGG , CM000679.2:g.27764946_27764948delinsTGG	GRCh38
NC_000017.10:g.26091972_26091974delinsTGG , CM000679.1:g.26091972_26091974delinsTGG	GRCh37
NC_000017.9:g.23116099_23116101delinsTGG	NCBI36
NG_011470.1:g.40582_40584delinsCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697337.1:c.*3092+659_*3092+661delinsCCA	ENSP00000513259.1:n.*3092+659_*3092+661delinsCCA
ENST00000697338.1:c.2276+587_2276+589delinsCCA	ENSP00000513260.1:n.2276+587_2276+589delinsCCA
ENST00000697339.1:c.1390+659_1390+661delinsCCA	ENSP00000513261.1:n.1390+659_1390+661delinsCCA
ENST00000697340.1:c.*1145+587_*1145+589delinsCCA	ENSP00000513262.1:n.*1145+587_*1145+589delinsCCA
ENST00000697341.1:n.2398+587_2398+589delinsCCA
ENST00000313735.11:c.2428+587_2428+589delinsCCA MANE Select	ENSP00000327251.6:n.2428+587_2428+589delinsCCA
ENST00000646938.1:c.2425+587_2425+589delinsCCA	ENSP00000494870.1:n.2425+587_2425+589delinsCCA
ENST00000313735.10:c.2428+587_2428+589delinsCCA	ENSP00000327251.6:n.2428+587_2428+589delinsCCA
ENST00000621962.1:c.2311+587_2311+589delinsCCA	ENSP00000482291.1:n.2311+587_2311+589delinsCCA
NM_000625.4:c.2428+587_2428+589delinsCCA MANE Select	NP_000616.3:n.2428+587_2428+589delinsCCA
XM_011524859.1:c.2428+587_2428+589delinsCCA	XP_011523161.1:n.2428+587_2428+589delinsCCA
XM_011524860.1:c.2425+587_2425+589delinsCCA	XP_011523162.1:n.2425+587_2425+589delinsCCA
XM_011524861.1:c.2356+659_2356+661delinsCCA	XP_011523163.1:n.2356+659_2356+661delinsCCA
XM_011524862.1:c.1762+587_1762+589delinsCCA	XP_011523164.1:n.1762+587_1762+589delinsCCA