Canonical Allele Identifier: CA349018619

Gene: SCN2A

Linked Data

• MyVariant Identifiers: chr2:g.166167059T>G (hg19) ; chr2:g.165310549T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165310549T>G , CM000664.2:g.165310549T>G	GRCh38
NC_000002.11:g.166167059T>G , CM000664.1:g.166167059T>G	GRCh37
NC_000002.10:g.165875305T>G	NCBI36
NG_008143.1:g.76148T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000631182.3:c.924T>G MANE Plus Clinical	ENSP00000486885.1:p.Asn308Lys
ENST00000375437.7:c.924T>G MANE Select	ENSP00000364586.2:p.Asn308Lys
ENST00000635945.1:n.1287T>G
ENST00000636071.2:c.924T>G	ENSP00000490107.1:p.Asn308Lys
ENST00000636135.1:c.795T>G	ENSP00000489821.1:p.Asn265Lys
ENST00000636384.2:c.924T>G	ENSP00000490765.1:p.Asn308Lys
ENST00000636662.2:c.*1447T>G	ENSP00000489873.1:n.*1447T>G
ENST00000636769.1:c.924T>G	ENSP00000490800.1:p.Asn308Lys
ENST00000636985.2:c.528T>G	ENSP00000490849.1:p.Asn176Lys
ENST00000637266.2:c.924T>G	ENSP00000490866.1:p.Asn308Lys
ENST00000637367.1:c.*857T>G	ENSP00000490592.1:n.*857T>G
ENST00000638151.1:n.1008T>G
ENST00000283256.10:c.924T>G	ENSP00000283256.6:p.Asn308Lys
ENST00000375427.4:c.924T>G	ENSP00000364576.2:p.Asn308Lys
ENST00000375437.6:c.924T>G	ENSP00000364586.2:p.Asn308Lys
ENST00000424833.5:c.924T>G	ENSP00000406454.2:p.Asn308Lys
ENST00000480032.4:n.1067T>G
ENST00000486878.2:c.465T>G	ENSP00000487466.1:p.Asn155Lys
ENST00000631182.2:c.924T>G	ENSP00000486885.1:p.Asn308Lys
NM_001040142.1:c.924T>G	NP_001035232.1:p.Asn308Lys
NM_001040143.1:c.924T>G	NP_001035233.1:p.Asn308Lys
NM_021007.2:c.924T>G	NP_066287.2:p.Asn308Lys
XM_005246750.2:c.924T>G	XP_005246807.1:p.Asn308Lys
XM_005246753.2:c.924T>G	XP_005246810.1:p.Asn308Lys
XM_005246754.3:c.894T>G	XP_005246811.1:p.Asn298Lys
XM_005246755.3:c.171T>G	XP_005246812.1:p.Asn57Lys
XM_011511608.1:c.924T>G	XP_011509910.1:p.Asn308Lys
XM_011511609.1:c.924T>G	XP_011509911.1:p.Asn308Lys
XM_005246753.3:c.924T>G	XP_005246810.1:p.Asn308Lys
XM_017004656.1:c.924T>G	XP_016860145.1:p.Asn308Lys
XM_017004657.1:c.924T>G	XP_016860146.1:p.Asn308Lys
XM_017004658.1:c.171T>G	XP_016860147.1:p.Asn57Lys
XM_024453037.1:c.171T>G	XP_024308805.1:p.Asn57Lys
NM_001040142.2:c.924T>G MANE Select	NP_001035232.1:p.Asn308Lys
NM_001040143.2:c.924T>G	NP_001035233.1:p.Asn308Lys
NM_001371246.1:c.924T>G MANE Plus Clinical	NP_001358175.1:p.Asn308Lys
NM_001371247.1:c.924T>G	NP_001358176.1:p.Asn308Lys
NM_021007.3:c.924T>G	NP_066287.2:p.Asn308Lys