Canonical Allele Identifier: CA2636789629
Gene: NOS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27782132_27782133insAAAACAAAAATAAAAACAAACAAACAAACAAAAAGAAAA , CM000679.2:g.27782132_27782133insAAAACAAAAATAAAAACAAACAAACAAACAAAAAGAAAA GRCh38
NC_000017.10:g.26109158_26109159insAAAACAAAAATAAAAACAAACAAACAAACAAAAAGAAAA , CM000679.1:g.26109158_26109159insAAAACAAAAATAAAAACAAACAAACAAACAAAAAGAAAA GRCh37
NC_000017.9:g.23133285_23133286insAAAACAAAAATAAAAACAAACAAACAAACAAAAAGAAAA NCBI36
NG_011470.1:g.23397_23398insTTTTCTTTTTGTTTGTTTGTTTGTTTTTATTTTTGTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000697337.1:c.*77-27_*77-26insTTTTCTTTTTGTTTGTTTGTTTGTTTTTATTTTTGTTTT ENSP00000513259.1:n.*77-27_*77-26insTTTTCTTTTTGTTTGTTTGTTTGTT...
ENST00000697338.1:c.479-27_479-26insTTTTCTTTTTGTTTGTTTGTTTGTTTTTATTTTTGTTTT ENSP00000513260.1:n.479-27_479-26insTTTTCTTTTTGTTTGTTTGTTTGTT...
ENST00000697339.1:c.315+6676_315+6677insTTTTCTTTTTGTTTGTTTGTTTGTTTTTATTTTTGTTTT ENSP00000513261.1:n.315+6676_315+6677insTTTTCTTTTTGTTTGTTTGTT...
ENST00000697340.1:c.628-27_628-26insTTTTCTTTTTGTTTGTTTGTTTGTTTTTATTTTTGTTTT ENSP00000513262.1:n.628-27_628-26insTTTTCTTTTTGTTTGTTTGTTTGTT...
ENST00000697341.1:n.601-27_601-26insTTTTCTTTTTGTTTGTTTGTTTGTTTTTATTTTTGTTTT
ENST00000313735.11:c.631-27_631-26insTTTTCTTTTTGTTTGTTTGTTTGTTTTTATTTTTGTTTT MANE Select ENSP00000327251.6:n.631-27_631-26insTTTTCTTTTTGTTTGTTTGTTTGTT...
ENST00000646938.1:c.628-27_628-26insTTTTCTTTTTGTTTGTTTGTTTGTTTTTATTTTTGTTTT ENSP00000494870.1:n.628-27_628-26insTTTTCTTTTTGTTTGTTTGTTTGTT...
ENST00000313735.10:c.631-27_631-26insTTTTCTTTTTGTTTGTTTGTTTGTTTTTATTTTTGTTTT ENSP00000327251.6:n.631-27_631-26insTTTTCTTTTTGTTTGTTTGTTTGTT...
ENST00000621962.1:c.631-27_631-26insTTTTCTTTTTGTTTGTTTGTTTGTTTTTATTTTTGTTTT ENSP00000482291.1:n.631-27_631-26insTTTTCTTTTTGTTTGTTTGTTTGTT...
NM_000625.4:c.631-27_631-26insTTTTCTTTTTGTTTGTTTGTTTGTTTTTATTTTTGTTTT MANE Select NP_000616.3:n.631-27_631-26insTTTTCTTTTTGTTTGTTTGTTTGTTTTTATT...
XM_011524859.1:c.631-27_631-26insTTTTCTTTTTGTTTGTTTGTTTGTTTTTATTTTTGTTTT XP_011523161.1:n.631-27_631-26insTTTTCTTTTTGTTTGTTTGTTTGTTTTT...
XM_011524860.1:c.628-27_628-26insTTTTCTTTTTGTTTGTTTGTTTGTTTTTATTTTTGTTTT XP_011523162.1:n.628-27_628-26insTTTTCTTTTTGTTTGTTTGTTTGTTTTT...
XM_011524861.1:c.631-27_631-26insTTTTCTTTTTGTTTGTTTGTTTGTTTTTATTTTTGTTTT XP_011523163.1:n.631-27_631-26insTTTTCTTTTTGTTTGTTTGTTTGTTTTT...
XM_011524862.1:c.-36-27_-36-26insTTTTCTTTTTGTTTGTTTGTTTGTTTTTATTTTTGTTTT XP_011523164.1:n.-36-27_-36-26insTTTTCTTTTTGTTTGTTTGTTTGTTTTT...