Canonical Allele Identifier: CA349017546

Gene: SCN2A

Linked Data

• MyVariant Identifiers: chr2:g.166165931G>T (hg19) ; chr2:g.165309421G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165309421G>T , CM000664.2:g.165309421G>T	GRCh38
NC_000002.11:g.166165931G>T , CM000664.1:g.166165931G>T	GRCh37
NC_000002.10:g.165874177G>T	NCBI36
NG_008143.1:g.75020G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000631182.3:c.697+165G>T MANE Plus Clinical	ENSP00000486885.1:n.697+165G>T
ENST00000375437.7:c.675G>T MANE Select	ENSP00000364586.2:p.Leu225Phe
ENST00000635945.1:n.1038G>T
ENST00000636071.2:c.697+165G>T	ENSP00000490107.1:n.697+165G>T
ENST00000636135.1:c.546G>T	ENSP00000489821.1:p.Leu182Phe
ENST00000636384.2:c.675G>T	ENSP00000490765.1:p.Leu225Phe
ENST00000636662.2:c.*1198G>T	ENSP00000489873.1:n.*1198G>T
ENST00000636769.1:c.675G>T	ENSP00000490800.1:p.Leu225Phe
ENST00000636985.2:c.279G>T	ENSP00000490849.1:p.Leu93Phe
ENST00000637266.2:c.675G>T	ENSP00000490866.1:p.Leu225Phe
ENST00000637367.1:c.*608G>T	ENSP00000490592.1:n.*608G>T
ENST00000638151.1:n.759G>T
ENST00000283256.10:c.675G>T	ENSP00000283256.6:p.Leu225Phe
ENST00000375427.4:c.697+165G>T	ENSP00000364576.2:n.697+165G>T
ENST00000375437.6:c.675G>T	ENSP00000364586.2:p.Leu225Phe
ENST00000424833.5:c.675G>T	ENSP00000406454.2:p.Leu225Phe
ENST00000480032.4:n.818G>T
ENST00000486878.2:c.216G>T	ENSP00000487466.1:p.Leu72Phe
ENST00000631182.2:c.697+165G>T	ENSP00000486885.1:n.697+165G>T
NM_001040142.1:c.675G>T	NP_001035232.1:p.Leu225Phe
NM_001040143.1:c.697+165G>T	NP_001035233.1:n.697+165G>T
NM_021007.2:c.675G>T	NP_066287.2:p.Leu225Phe
XM_005246750.2:c.675G>T	XP_005246807.1:p.Leu225Phe
XM_005246753.2:c.697+165G>T	XP_005246810.1:n.697+165G>T
XM_005246754.3:c.645G>T	XP_005246811.1:p.Leu215Phe
XM_005246755.3:c.-57+627G>T	XP_005246812.1:n.-57+627G>T
XM_011511608.1:c.675G>T	XP_011509910.1:p.Leu225Phe
XM_011511609.1:c.675G>T	XP_011509911.1:p.Leu225Phe
XM_005246753.3:c.697+165G>T	XP_005246810.1:n.697+165G>T
XM_017004656.1:c.675G>T	XP_016860145.1:p.Leu225Phe
XM_017004657.1:c.697+165G>T	XP_016860146.1:n.697+165G>T
XM_017004658.1:c.-79G>T	XP_016860147.1:n.-79G>T
XM_024453037.1:c.-57+627G>T	XP_024308805.1:n.-57+627G>T
NM_001040142.2:c.675G>T MANE Select	NP_001035232.1:p.Leu225Phe
NM_001040143.2:c.697+165G>T	NP_001035233.1:n.697+165G>T
NM_001371246.1:c.697+165G>T MANE Plus Clinical	NP_001358175.1:n.697+165G>T
NM_001371247.1:c.675G>T	NP_001358176.1:p.Leu225Phe
NM_021007.3:c.675G>T	NP_066287.2:p.Leu225Phe