Canonical Allele Identifier: CA2636788193
Gene: NOS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27769278_27769279insAGAAGGGGGTCCAGCT , CM000679.2:g.27769278_27769279insAGAAGGGGGTCCAGCT GRCh38
NC_000017.10:g.26096304_26096305insAGAAGGGGGTCCAGCT , CM000679.1:g.26096304_26096305insAGAAGGGGGTCCAGCT GRCh37
NC_000017.9:g.23120431_23120432insAGAAGGGGGTCCAGCT NCBI36
NG_011470.1:g.36251_36252insAGCTGGACCCCCTTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000697337.1:c.*2596-128_*2596-127insAGCTGGACCCCCTTCT ENSP00000513259.1:n.*2596-128_*2596-127insAGCTGGACCCCCTTCT
ENST00000697338.1:c.1708-128_1708-127insAGCTGGACCCCCTTCT ENSP00000513260.1:n.1708-128_1708-127insAGCTGGACCCCCTTCT
ENST00000697339.1:c.894-128_894-127insAGCTGGACCCCCTTCT ENSP00000513261.1:n.894-128_894-127insAGCTGGACCCCCTTCT
ENST00000697340.1:c.*577-128_*577-127insAGCTGGACCCCCTTCT ENSP00000513262.1:n.*577-128_*577-127insAGCTGGACCCCCTTCT
ENST00000697341.1:n.1830-128_1830-127insAGCTGGACCCCCTTCT
ENST00000313735.11:c.1860-128_1860-127insAGCTGGACCCCCTTCT MANE Select ENSP00000327251.6:n.1860-128_1860-127insAGCTGGACCCCCTTCT
ENST00000646938.1:c.1857-128_1857-127insAGCTGGACCCCCTTCT ENSP00000494870.1:n.1857-128_1857-127insAGCTGGACCCCCTTCT
ENST00000313735.10:c.1860-128_1860-127insAGCTGGACCCCCTTCT ENSP00000327251.6:n.1860-128_1860-127insAGCTGGACCCCCTTCT
ENST00000621962.1:c.1743-128_1743-127insAGCTGGACCCCCTTCT ENSP00000482291.1:n.1743-128_1743-127insAGCTGGACCCCCTTCT
NM_000625.4:c.1860-128_1860-127insAGCTGGACCCCCTTCT MANE Select NP_000616.3:n.1860-128_1860-127insAGCTGGACCCCCTTCT
XM_011524859.1:c.1860-128_1860-127insAGCTGGACCCCCTTCT XP_011523161.1:n.1860-128_1860-127insAGCTGGACCCCCTTCT
XM_011524860.1:c.1857-128_1857-127insAGCTGGACCCCCTTCT XP_011523162.1:n.1857-128_1857-127insAGCTGGACCCCCTTCT
XM_011524861.1:c.1860-128_1860-127insAGCTGGACCCCCTTCT XP_011523163.1:n.1860-128_1860-127insAGCTGGACCCCCTTCT
XM_011524862.1:c.1194-128_1194-127insAGCTGGACCCCCTTCT XP_011523164.1:n.1194-128_1194-127insAGCTGGACCCCCTTCT