Canonical Allele Identifier: CA302728183
Gene: NETO1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.72774833C>T , CM000680.2:g.72774833C>T GRCh38
NC_000018.9:g.70442068C>T , CM000680.1:g.70442068C>T GRCh37
NC_000018.8:g.68593048C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000327305.11:c.868+8845G>A MANE Select ENSP00000313088.6:n.868+8845G>A
ENST00000327305.10:c.868+8845G>A ENSP00000313088.6:n.868+8845G>A
ENST00000583169.5:c.868+8845G>A ENSP00000464312.1:n.868+8845G>A
NM_001201465.1:c.868+8845G>A NP_001188394.1:n.868+8845G>A
NM_138966.3:c.868+8845G>A NP_620416.1:n.868+8845G>A
XM_005266774.3:c.868+8845G>A XP_005266831.1:n.868+8845G>A
XM_005266776.3:c.868+8845G>A XP_005266833.1:n.868+8845G>A
XM_011526218.1:c.868+8845G>A XP_011524520.1:n.868+8845G>A
XR_935254.1:n.930+8845G>A
XR_935255.1:n.930+8845G>A
XR_935256.1:n.421+8845G>A
XR_935257.1:n.546+8845G>A
NM_001201465.2:c.868+8845G>A NP_001188394.1:n.868+8845G>A
NM_001354017.1:c.868+8845G>A NP_001340946.1:n.868+8845G>A
NM_001354018.1:c.442+8845G>A NP_001340947.1:n.442+8845G>A
NM_001354020.1:c.844+8845G>A NP_001340949.1:n.844+8845G>A
NM_138966.4:c.868+8845G>A NP_620416.1:n.868+8845G>A
NR_148694.1:n.1249+8845G>A
NR_148695.1:n.1294+8845G>A
XM_017026017.1:c.868+8845G>A XP_016881506.1:n.868+8845G>A
XM_017026018.1:c.868+8845G>A XP_016881507.1:n.868+8845G>A
XM_017026019.1:c.844+8845G>A XP_016881508.1:n.844+8845G>A
NM_138966.5:c.868+8845G>A MANE Select NP_620416.2:n.868+8845G>A
NM_001201465.3:c.868+8845G>A NP_001188394.2:n.868+8845G>A
NM_001354017.2:c.868+8845G>A NP_001340946.2:n.868+8845G>A
NM_001354018.2:c.442+8845G>A NP_001340947.2:n.442+8845G>A
NR_148694.2:n.1564+8845G>A
NM_001354020.2:c.844+8845G>A NP_001340949.2:n.844+8845G>A
NR_148695.2:n.1294+8845G>A
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