Canonical Allele Identifier: CA1304563748
Gene: SCN2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.165386785C= , CM000664.2:g.165386785C= GRCh38
NC_000002.11:g.166243295C= , CM000664.1:g.166243295C= GRCh37
NC_000002.10:g.165951541C= NCBI36
NG_008143.1:g.152384C=

Transcript Alleles

HGVS Amino-acid change
ENST00000631182.3:c.4591C= MANE Plus Clinical ENSP00000486885.1:p.Gln1531=
ENST00000375437.7:c.4591C= MANE Select ENSP00000364586.2:p.Gln1531=
ENST00000636071.2:c.4591C= ENSP00000490107.1:p.Gln1531=
ENST00000636135.1:c.*2910C= ENSP00000489821.1:n.*2910C=
ENST00000636384.2:c.*2578C= ENSP00000490765.1:n.*2578C=
ENST00000636662.2:c.*5114C= ENSP00000489873.1:n.*5114C=
ENST00000636769.1:c.*2533C= ENSP00000490800.1:n.*2533C=
ENST00000636985.2:c.4195C= ENSP00000490849.1:p.Gln1399=
ENST00000637266.2:c.4591C= ENSP00000490866.1:p.Gln1531=
ENST00000283256.10:c.4591C= ENSP00000283256.6:p.Gln1531=
ENST00000375427.4:c.4591C= ENSP00000364576.2:p.Gln1531=
ENST00000375437.6:c.4591C= ENSP00000364586.2:p.Gln1531=
ENST00000480032.4:n.8022C=
ENST00000631182.2:c.4591C= ENSP00000486885.1:p.Gln1531=
NM_001040142.1:c.4591C= NP_001035232.1:p.Gln1531=
NM_001040143.1:c.4591C= NP_001035233.1:p.Gln1531=
NM_021007.2:c.4591C= NP_066287.2:p.Gln1531=
XM_005246750.2:c.4591C= XP_005246807.1:p.Gln1531=
XM_005246753.2:c.4591C= XP_005246810.1:p.Gln1531=
XM_005246754.3:c.4561C= XP_005246811.1:p.Gln1521=
XM_005246755.3:c.3838C= XP_005246812.1:p.Gln1280=
XM_011511608.1:c.4591C= XP_011509910.1:p.Gln1531=
XM_011511609.1:c.4591C= XP_011509911.1:p.Gln1531=
XM_005246753.3:c.4591C= XP_005246810.1:p.Gln1531=
XM_017004656.1:c.4591C= XP_016860145.1:p.Gln1531=
XM_017004657.1:c.4591C= XP_016860146.1:p.Gln1531=
XM_017004658.1:c.3838C= XP_016860147.1:p.Gln1280=
XM_017004659.1:c.2389C= XP_016860148.1:p.Gln797=
XM_024453037.1:c.3838C= XP_024308805.1:p.Gln1280=
NM_001040142.2:c.4591C= MANE Select NP_001035232.1:p.Gln1531=
NM_001040143.2:c.4591C= NP_001035233.1:p.Gln1531=
NM_001371246.1:c.4591C= MANE Plus Clinical NP_001358175.1:p.Gln1531=
NM_001371247.1:c.4591C= NP_001358176.1:p.Gln1531=
NM_021007.3:c.4591C= NP_066287.2:p.Gln1531=