Canonical Allele Identifier: CA2254020885

Gene: NOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27797630_27797631delinsTG , CM000679.2:g.27797630_27797631delinsTG	GRCh38
NC_000017.10:g.26124656_26124657delinsTG , CM000679.1:g.26124656_26124657delinsTG	GRCh37
NC_000017.9:g.23148783_23148784delinsTG	NCBI36
NG_011470.1:g.7899_7900delinsCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000697337.1:c.110+1069_110+1070delinsCA	ENSP00000513259.1:n.110+1069_110+1070delinsCA
ENST00000313735.11:c.110+1069_110+1070delinsCA MANE Select	ENSP00000327251.6:n.110+1069_110+1070delinsCA
ENST00000313735.10:c.110+1069_110+1070delinsCA	ENSP00000327251.6:n.110+1069_110+1070delinsCA
ENST00000621962.1:c.110+1069_110+1070delinsCA	ENSP00000482291.1:n.110+1069_110+1070delinsCA
NM_000625.4:c.110+1069_110+1070delinsCA MANE Select	NP_000616.3:n.110+1069_110+1070delinsCA
XM_011524859.1:c.110+1069_110+1070delinsCA	XP_011523161.1:n.110+1069_110+1070delinsCA
XM_011524861.1:c.110+1069_110+1070delinsCA	XP_011523163.1:n.110+1069_110+1070delinsCA