Canonical Allele Identifier: CA2753007151
Gene: SCN2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.165309525_165309526insTTTTTACATATTTATTTGCAATATGCAACT , CM000664.2:g.165309525_165309526insTTTTTACATATTTATTTGCAATATGCAACT GRCh38
NC_000002.11:g.166166035_166166036insTTTTTACATATTTATTTGCAATATGCAACT , CM000664.1:g.166166035_166166036insTTTTTACATATTTATTTGCAATATGCAACT GRCh37
NC_000002.10:g.165874281_165874282insTTTTTACATATTTATTTGCAATATGCAACT NCBI36
NG_008143.1:g.75124_75125insTTTTTACATATTTATTTGCAATATGCAACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000631182.3:c.697+269_697+270insTTTTTACATATTTATTTGCAATATGCAACT MANE Plus Clinical ENSP00000486885.1:n.697+269_697+270insTTTTTACATATTTATTTGCAATA...
ENST00000375437.7:c.697+82_697+83insTTTTTACATATTTATTTGCAATATGCAACT MANE Select ENSP00000364586.2:n.697+82_697+83insTTTTTACATATTTATTTGCAATATG...
ENST00000635945.1:n.1060+82_1060+83insTTTTTACATATTTATTTGCAATATGCAACT
ENST00000636071.2:c.697+269_697+270insTTTTTACATATTTATTTGCAATATGCAACT ENSP00000490107.1:n.697+269_697+270insTTTTTACATATTTATTTGCAATA...
ENST00000636135.1:c.568+82_568+83insTTTTTACATATTTATTTGCAATATGCAACT ENSP00000489821.1:n.568+82_568+83insTTTTTACATATTTATTTGCAATATG...
ENST00000636384.2:c.697+82_697+83insTTTTTACATATTTATTTGCAATATGCAACT ENSP00000490765.1:n.697+82_697+83insTTTTTACATATTTATTTGCAATATG...
ENST00000636662.2:c.*1220+82_*1220+83insTTTTTACATATTTATTTGCAATATGCAACT ENSP00000489873.1:n.*1220+82_*1220+83insTTTTTACATATTTATTTGCAA...
ENST00000636769.1:c.697+82_697+83insTTTTTACATATTTATTTGCAATATGCAACT ENSP00000490800.1:n.697+82_697+83insTTTTTACATATTTATTTGCAATATG...
ENST00000636985.2:c.301+82_301+83insTTTTTACATATTTATTTGCAATATGCAACT ENSP00000490849.1:n.301+82_301+83insTTTTTACATATTTATTTGCAATATG...
ENST00000637266.2:c.697+82_697+83insTTTTTACATATTTATTTGCAATATGCAACT ENSP00000490866.1:n.697+82_697+83insTTTTTACATATTTATTTGCAATATG...
ENST00000637367.1:c.*630+82_*630+83insTTTTTACATATTTATTTGCAATATGCAACT ENSP00000490592.1:n.*630+82_*630+83insTTTTTACATATTTATTTGCAATA...
ENST00000638151.1:n.781+82_781+83insTTTTTACATATTTATTTGCAATATGCAACT
ENST00000283256.10:c.697+82_697+83insTTTTTACATATTTATTTGCAATATGCAACT ENSP00000283256.6:n.697+82_697+83insTTTTTACATATTTATTTGCAATATG...
ENST00000375427.4:c.697+269_697+270insTTTTTACATATTTATTTGCAATATGCAACT ENSP00000364576.2:n.697+269_697+270insTTTTTACATATTTATTTGCAATA...
ENST00000375437.6:c.697+82_697+83insTTTTTACATATTTATTTGCAATATGCAACT ENSP00000364586.2:n.697+82_697+83insTTTTTACATATTTATTTGCAATATG...
ENST00000424833.5:c.697+82_697+83insTTTTTACATATTTATTTGCAATATGCAACT ENSP00000406454.2:n.697+82_697+83insTTTTTACATATTTATTTGCAATATG...
ENST00000480032.4:n.840+82_840+83insTTTTTACATATTTATTTGCAATATGCAACT
ENST00000486878.2:c.238+82_238+83insTTTTTACATATTTATTTGCAATATGCAACT ENSP00000487466.1:n.238+82_238+83insTTTTTACATATTTATTTGCAATATG...
ENST00000631182.2:c.697+269_697+270insTTTTTACATATTTATTTGCAATATGCAACT ENSP00000486885.1:n.697+269_697+270insTTTTTACATATTTATTTGCAATA...
NM_001040142.1:c.697+82_697+83insTTTTTACATATTTATTTGCAATATGCAACT NP_001035232.1:n.697+82_697+83insTTTTTACATATTTATTTGCAATATGCAA...
NM_001040143.1:c.697+269_697+270insTTTTTACATATTTATTTGCAATATGCAACT NP_001035233.1:n.697+269_697+270insTTTTTACATATTTATTTGCAATATGC...
NM_021007.2:c.697+82_697+83insTTTTTACATATTTATTTGCAATATGCAACT NP_066287.2:n.697+82_697+83insTTTTTACATATTTATTTGCAATATGCAACT
XM_005246750.2:c.697+82_697+83insTTTTTACATATTTATTTGCAATATGCAACT XP_005246807.1:n.697+82_697+83insTTTTTACATATTTATTTGCAATATGCAA...
XM_005246753.2:c.697+269_697+270insTTTTTACATATTTATTTGCAATATGCAACT XP_005246810.1:n.697+269_697+270insTTTTTACATATTTATTTGCAATATGC...
XM_005246754.3:c.667+82_667+83insTTTTTACATATTTATTTGCAATATGCAACT XP_005246811.1:n.667+82_667+83insTTTTTACATATTTATTTGCAATATGCAA...
XM_005246755.3:c.-57+731_-57+732insTTTTTACATATTTATTTGCAATATGCAACT XP_005246812.1:n.-57+731_-57+732insTTTTTACATATTTATTTGCAATATGC...
XM_011511608.1:c.697+82_697+83insTTTTTACATATTTATTTGCAATATGCAACT XP_011509910.1:n.697+82_697+83insTTTTTACATATTTATTTGCAATATGCAA...
XM_011511609.1:c.697+82_697+83insTTTTTACATATTTATTTGCAATATGCAACT XP_011509911.1:n.697+82_697+83insTTTTTACATATTTATTTGCAATATGCAA...
XM_005246753.3:c.697+269_697+270insTTTTTACATATTTATTTGCAATATGCAACT XP_005246810.1:n.697+269_697+270insTTTTTACATATTTATTTGCAATATGC...
XM_017004656.1:c.697+82_697+83insTTTTTACATATTTATTTGCAATATGCAACT XP_016860145.1:n.697+82_697+83insTTTTTACATATTTATTTGCAATATGCAA...
XM_017004657.1:c.697+269_697+270insTTTTTACATATTTATTTGCAATATGCAACT XP_016860146.1:n.697+269_697+270insTTTTTACATATTTATTTGCAATATGC...
XM_017004658.1:c.-57+82_-57+83insTTTTTACATATTTATTTGCAATATGCAACT XP_016860147.1:n.-57+82_-57+83insTTTTTACATATTTATTTGCAATATGCAA...
XM_024453037.1:c.-57+731_-57+732insTTTTTACATATTTATTTGCAATATGCAACT XP_024308805.1:n.-57+731_-57+732insTTTTTACATATTTATTTGCAATATGC...
NM_001040142.2:c.697+82_697+83insTTTTTACATATTTATTTGCAATATGCAACT MANE Select NP_001035232.1:n.697+82_697+83insTTTTTACATATTTATTTGCAATATGCAA...
NM_001040143.2:c.697+269_697+270insTTTTTACATATTTATTTGCAATATGCAACT NP_001035233.1:n.697+269_697+270insTTTTTACATATTTATTTGCAATATGC...
NM_001371246.1:c.697+269_697+270insTTTTTACATATTTATTTGCAATATGCAACT MANE Plus Clinical NP_001358175.1:n.697+269_697+270insTTTTTACATATTTATTTGCAATATGC...
NM_001371247.1:c.697+82_697+83insTTTTTACATATTTATTTGCAATATGCAACT NP_001358176.1:n.697+82_697+83insTTTTTACATATTTATTTGCAATATGCAA...
NM_021007.3:c.697+82_697+83insTTTTTACATATTTATTTGCAATATGCAACT NP_066287.2:n.697+82_697+83insTTTTTACATATTTATTTGCAATATGCAACT