Canonical Allele Identifier: CA349036805

Gene: SCN2A

Linked Data

• dbSNP Id: rs1574747169
• MyVariant Identifiers: chr2:g.166243476C>G (hg19) ; chr2:g.165386966C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165386966C>G , CM000664.2:g.165386966C>G	GRCh38
NC_000002.11:g.166243476C>G , CM000664.1:g.166243476C>G	GRCh37
NC_000002.10:g.165951722C>G	NCBI36
NG_008143.1:g.152565C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000631182.3:c.4772C>G MANE Plus Clinical	ENSP00000486885.1:p.Thr1591Ser
ENST00000375437.7:c.4772C>G MANE Select	ENSP00000364586.2:p.Thr1591Ser
ENST00000636071.2:c.4772C>G	ENSP00000490107.1:p.Thr1591Ser
ENST00000636135.1:c.*3091C>G	ENSP00000489821.1:n.*3091C>G
ENST00000636384.2:c.*2759C>G	ENSP00000490765.1:n.*2759C>G
ENST00000636662.2:c.*5295C>G	ENSP00000489873.1:n.*5295C>G
ENST00000636769.1:c.*2714C>G	ENSP00000490800.1:n.*2714C>G
ENST00000636985.2:c.4376C>G	ENSP00000490849.1:p.Thr1459Ser
ENST00000637266.2:c.4772C>G	ENSP00000490866.1:p.Thr1591Ser
ENST00000283256.10:c.4772C>G	ENSP00000283256.6:p.Thr1591Ser
ENST00000375427.4:c.4772C>G	ENSP00000364576.2:p.Thr1591Ser
ENST00000375437.6:c.4772C>G	ENSP00000364586.2:p.Thr1591Ser
ENST00000480032.4:n.8203C>G
ENST00000631182.2:c.4772C>G	ENSP00000486885.1:p.Thr1591Ser
NM_001040142.1:c.4772C>G	NP_001035232.1:p.Thr1591Ser
NM_001040143.1:c.4772C>G	NP_001035233.1:p.Thr1591Ser
NM_021007.2:c.4772C>G	NP_066287.2:p.Thr1591Ser
XM_005246750.2:c.4772C>G	XP_005246807.1:p.Thr1591Ser
XM_005246753.2:c.4772C>G	XP_005246810.1:p.Thr1591Ser
XM_005246754.3:c.4742C>G	XP_005246811.1:p.Thr1581Ser
XM_005246755.3:c.4019C>G	XP_005246812.1:p.Thr1340Ser
XM_011511608.1:c.4772C>G	XP_011509910.1:p.Thr1591Ser
XM_011511609.1:c.4772C>G	XP_011509911.1:p.Thr1591Ser
XM_005246753.3:c.4772C>G	XP_005246810.1:p.Thr1591Ser
XM_017004656.1:c.4772C>G	XP_016860145.1:p.Thr1591Ser
XM_017004657.1:c.4772C>G	XP_016860146.1:p.Thr1591Ser
XM_017004658.1:c.4019C>G	XP_016860147.1:p.Thr1340Ser
XM_017004659.1:c.2570C>G	XP_016860148.1:p.Thr857Ser
XM_024453037.1:c.4019C>G	XP_024308805.1:p.Thr1340Ser
NM_001040142.2:c.4772C>G MANE Select	NP_001035232.1:p.Thr1591Ser
NM_001040143.2:c.4772C>G	NP_001035233.1:p.Thr1591Ser
NM_001371246.1:c.4772C>G MANE Plus Clinical	NP_001358175.1:p.Thr1591Ser
NM_001371247.1:c.4772C>G	NP_001358176.1:p.Thr1591Ser
NM_021007.3:c.4772C>G	NP_066287.2:p.Thr1591Ser