Canonical Allele Identifier: CA2254006477

Gene: NOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27764928_27764930delinsTCA , CM000679.2:g.27764928_27764930delinsTCA	GRCh38
NC_000017.10:g.26091954_26091956delinsTCA , CM000679.1:g.26091954_26091956delinsTCA	GRCh37
NC_000017.9:g.23116081_23116083delinsTCA	NCBI36
NG_011470.1:g.40600_40602delinsTGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000697337.1:c.*3092+677_*3092+679delinsTGA	ENSP00000513259.1:n.*3092+677_*3092+679de...
ENST00000697338.1:c.2276+605_2276+607delinsTGA	ENSP00000513260.1:n.2276+605_2276+607deli...
ENST00000697339.1:c.1390+677_1390+679delinsTGA	ENSP00000513261.1:n.1390+677_1390+679deli...
ENST00000697340.1:c.*1145+605_*1145+607delinsTGA	ENSP00000513262.1:n.*1145+605_*1145+607de...
ENST00000697341.1:n.2398+605_2398+607delinsTGA
ENST00000313735.11:c.2428+605_2428+607delinsTGA MANE Select	ENSP00000327251.6:n.2428+605_2428+607deli...
ENST00000646938.1:c.2425+605_2425+607delinsTGA	ENSP00000494870.1:n.2425+605_2425+607deli...
ENST00000313735.10:c.2428+605_2428+607delinsTGA	ENSP00000327251.6:n.2428+605_2428+607deli...
ENST00000621962.1:c.2311+605_2311+607delinsTGA	ENSP00000482291.1:n.2311+605_2311+607deli...
NM_000625.4:c.2428+605_2428+607delinsTGA MANE Select	NP_000616.3:n.2428+605_2428+607delinsTGA
XM_011524859.1:c.2428+605_2428+607delinsTGA	XP_011523161.1:n.2428+605_2428+607delinsT...
XM_011524860.1:c.2425+605_2425+607delinsTGA	XP_011523162.1:n.2425+605_2425+607delinsT...
XM_011524861.1:c.2356+677_2356+679delinsTGA	XP_011523163.1:n.2356+677_2356+679delinsT...
XM_011524862.1:c.1762+605_1762+607delinsTGA	XP_011523164.1:n.1762+605_1762+607delinsT...