Canonical Allele Identifier: CA349017461

Gene: SCN2A

Linked Data

• MyVariant Identifiers: chr2:g.166165908A>T (hg19) ; chr2:g.165309398A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165309398A>T , CM000664.2:g.165309398A>T	GRCh38
NC_000002.11:g.166165908A>T , CM000664.1:g.166165908A>T	GRCh37
NC_000002.10:g.165874154A>T	NCBI36
NG_008143.1:g.74997A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000631182.3:c.697+142A>T MANE Plus Clinical	ENSP00000486885.1:n.697+142A>T
ENST00000375437.7:c.652A>T MANE Select	ENSP00000364586.2:p.Thr218Ser
ENST00000635945.1:n.1015A>T
ENST00000636071.2:c.697+142A>T	ENSP00000490107.1:n.697+142A>T
ENST00000636135.1:c.523A>T	ENSP00000489821.1:p.Thr175Ser
ENST00000636384.2:c.652A>T	ENSP00000490765.1:p.Thr218Ser
ENST00000636662.2:c.*1175A>T	ENSP00000489873.1:n.*1175A>T
ENST00000636769.1:c.652A>T	ENSP00000490800.1:p.Thr218Ser
ENST00000636985.2:c.256A>T	ENSP00000490849.1:p.Thr86Ser
ENST00000637266.2:c.652A>T	ENSP00000490866.1:p.Thr218Ser
ENST00000637367.1:c.*585A>T	ENSP00000490592.1:n.*585A>T
ENST00000638151.1:n.736A>T
ENST00000283256.10:c.652A>T	ENSP00000283256.6:p.Thr218Ser
ENST00000375427.4:c.697+142A>T	ENSP00000364576.2:n.697+142A>T
ENST00000375437.6:c.652A>T	ENSP00000364586.2:p.Thr218Ser
ENST00000424833.5:c.652A>T	ENSP00000406454.2:p.Thr218Ser
ENST00000480032.4:n.795A>T
ENST00000486878.2:c.193A>T	ENSP00000487466.1:p.Thr65Ser
ENST00000631182.2:c.697+142A>T	ENSP00000486885.1:n.697+142A>T
NM_001040142.1:c.652A>T	NP_001035232.1:p.Thr218Ser
NM_001040143.1:c.697+142A>T	NP_001035233.1:n.697+142A>T
NM_021007.2:c.652A>T	NP_066287.2:p.Thr218Ser
XM_005246750.2:c.652A>T	XP_005246807.1:p.Thr218Ser
XM_005246753.2:c.697+142A>T	XP_005246810.1:n.697+142A>T
XM_005246754.3:c.622A>T	XP_005246811.1:p.Thr208Ser
XM_005246755.3:c.-57+604A>T	XP_005246812.1:n.-57+604A>T
XM_011511608.1:c.652A>T	XP_011509910.1:p.Thr218Ser
XM_011511609.1:c.652A>T	XP_011509911.1:p.Thr218Ser
XM_005246753.3:c.697+142A>T	XP_005246810.1:n.697+142A>T
XM_017004656.1:c.652A>T	XP_016860145.1:p.Thr218Ser
XM_017004657.1:c.697+142A>T	XP_016860146.1:n.697+142A>T
XM_017004658.1:c.-102A>T	XP_016860147.1:n.-102A>T
XM_024453037.1:c.-57+604A>T	XP_024308805.1:n.-57+604A>T
NM_001040142.2:c.652A>T MANE Select	NP_001035232.1:p.Thr218Ser
NM_001040143.2:c.697+142A>T	NP_001035233.1:n.697+142A>T
NM_001371246.1:c.697+142A>T MANE Plus Clinical	NP_001358175.1:n.697+142A>T
NM_001371247.1:c.652A>T	NP_001358176.1:p.Thr218Ser
NM_021007.3:c.652A>T	NP_066287.2:p.Thr218Ser