Canonical Allele Identifier: CA398301600
Gene: NOS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27769584T>C , CM000679.2:g.27769584T>C GRCh38
NC_000017.10:g.26096610T>C , CM000679.1:g.26096610T>C GRCh37
NC_000017.9:g.23120737T>C NCBI36
NG_011470.1:g.35946A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000697337.1:c.*2546A>G ENSP00000513259.1:n.*2546A>G
ENST00000697338.1:c.1658A>G ENSP00000513260.1:n.1658A>G
ENST00000697339.1:c.844A>G ENSP00000513261.1:p.Lys282Glu
ENST00000697340.1:c.*527A>G ENSP00000513262.1:n.*527A>G
ENST00000697341.1:n.1780A>G
ENST00000313735.11:c.1810A>G MANE Select ENSP00000327251.6:p.Lys604Glu
ENST00000646938.1:c.1807A>G ENSP00000494870.1:p.Lys603Glu
ENST00000313735.10:c.1810A>G ENSP00000327251.6:p.Lys604Glu
ENST00000621962.1:c.1693A>G ENSP00000482291.1:p.Lys565Glu
NM_000625.4:c.1810A>G MANE Select NP_000616.3:p.Lys604Glu
XM_011524859.1:c.1810A>G XP_011523161.1:p.Lys604Glu
XM_011524860.1:c.1807A>G XP_011523162.1:p.Lys603Glu
XM_011524861.1:c.1810A>G XP_011523163.1:p.Lys604Glu
XM_011524862.1:c.1144A>G XP_011523164.1:p.Lys382Glu