Canonical Allele Identifier: CA1304549990
Gene: SCN2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.165354272G= , CM000664.2:g.165354272G= GRCh38
NC_000002.11:g.166210782G= , CM000664.1:g.166210782G= GRCh37
NC_000002.10:g.165919028G= NCBI36
NG_008143.1:g.119871G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000631182.3:c.3000G= MANE Plus Clinical ENSP00000486885.1:p.Met1000=
ENST00000375437.7:c.3000G= MANE Select ENSP00000364586.2:p.Met1000=
ENST00000636071.2:c.3000G= ENSP00000490107.1:p.Met1000=
ENST00000636135.1:c.*1319G= ENSP00000489821.1:n.*1319G=
ENST00000636384.2:c.*987G= ENSP00000490765.1:n.*987G=
ENST00000636662.2:c.*3523G= ENSP00000489873.1:n.*3523G=
ENST00000636769.1:c.*942G= ENSP00000490800.1:n.*942G=
ENST00000636985.2:c.2604G= ENSP00000490849.1:p.Met868=
ENST00000637266.2:c.3000G= ENSP00000490866.1:p.Met1000=
ENST00000673831.1:c.746G= ENSP00000501305.1:n.746G=
ENST00000673883.1:c.565G= ENSP00000501309.1:n.565G=
ENST00000674133.1:c.851G=
ENST00000283256.10:c.3000G= ENSP00000283256.6:p.Met1000=
ENST00000375427.4:c.3000G= ENSP00000364576.2:p.Met1000=
ENST00000375437.6:c.3000G= ENSP00000364586.2:p.Met1000=
ENST00000480032.4:n.3143G=
ENST00000631182.2:c.3000G= ENSP00000486885.1:p.Met1000=
NM_001040142.1:c.3000G= NP_001035232.1:p.Met1000=
NM_001040143.1:c.3000G= NP_001035233.1:p.Met1000=
NM_021007.2:c.3000G= NP_066287.2:p.Met1000=
XM_005246750.2:c.3000G= XP_005246807.1:p.Met1000=
XM_005246753.2:c.3000G= XP_005246810.1:p.Met1000=
XM_005246754.3:c.2970G= XP_005246811.1:p.Met990=
XM_005246755.3:c.2247G= XP_005246812.1:p.Met749=
XM_011511608.1:c.3000G= XP_011509910.1:p.Met1000=
XM_011511609.1:c.3000G= XP_011509911.1:p.Met1000=
XM_005246753.3:c.3000G= XP_005246810.1:p.Met1000=
XM_017004656.1:c.3000G= XP_016860145.1:p.Met1000=
XM_017004657.1:c.3000G= XP_016860146.1:p.Met1000=
XM_017004658.1:c.2247G= XP_016860147.1:p.Met749=
XM_017004659.1:c.798G= XP_016860148.1:p.Met266=
XM_024453037.1:c.2247G= XP_024308805.1:p.Met749=
NM_001040142.2:c.3000G= MANE Select NP_001035232.1:p.Met1000=
NM_001040143.2:c.3000G= NP_001035233.1:p.Met1000=
NM_001371246.1:c.3000G= MANE Plus Clinical NP_001358175.1:p.Met1000=
NM_001371247.1:c.3000G= NP_001358176.1:p.Met1000=
NM_021007.3:c.3000G= NP_066287.2:p.Met1000=