Canonical Allele Identifier: CA1939710

Gene: SCN2A

Linked Data

• ClinVar Variation Id: 840602
• ClinVar RCV Id: RCV001042638
• dbSNP Id: rs754706708
• ExAC: 2:166167027 A / G
• gnomAD v2: 2-166167027-A-G
• gnomAD v3: 2-165310517-A-G
• gnomAD v4: 2-165310517-A-G
• MyVariant Identifiers: chr2:g.166167027A>G (hg19) ; chr2:g.165310517A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165310517A>G , CM000664.2:g.165310517A>G	GRCh38
NC_000002.11:g.166167027A>G , CM000664.1:g.166167027A>G	GRCh37
NC_000002.10:g.165875273A>G	NCBI36
NG_008143.1:g.76116A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000631182.3:c.892A>G MANE Plus Clinical	ENSP00000486885.1:p.Asn298Asp
ENST00000375437.7:c.892A>G MANE Select	ENSP00000364586.2:p.Asn298Asp
ENST00000635945.1:n.1255A>G
ENST00000636071.2:c.892A>G	ENSP00000490107.1:p.Asn298Asp
ENST00000636135.1:c.763A>G	ENSP00000489821.1:p.Asn255Asp
ENST00000636384.2:c.892A>G	ENSP00000490765.1:p.Asn298Asp
ENST00000636662.2:c.*1415A>G	ENSP00000489873.1:n.*1415A>G
ENST00000636769.1:c.892A>G	ENSP00000490800.1:p.Asn298Asp
ENST00000636985.2:c.496A>G	ENSP00000490849.1:p.Asn166Asp
ENST00000637266.2:c.892A>G	ENSP00000490866.1:p.Asn298Asp
ENST00000637367.1:c.*825A>G	ENSP00000490592.1:n.*825A>G
ENST00000638151.1:n.976A>G
ENST00000283256.10:c.892A>G	ENSP00000283256.6:p.Asn298Asp
ENST00000375427.4:c.892A>G	ENSP00000364576.2:p.Asn298Asp
ENST00000375437.6:c.892A>G	ENSP00000364586.2:p.Asn298Asp
ENST00000424833.5:c.892A>G	ENSP00000406454.2:p.Asn298Asp
ENST00000480032.4:n.1035A>G
ENST00000486878.2:c.433A>G	ENSP00000487466.1:p.Asn145Asp
ENST00000631182.2:c.892A>G	ENSP00000486885.1:p.Asn298Asp
NM_001040142.1:c.892A>G	NP_001035232.1:p.Asn298Asp
NM_001040143.1:c.892A>G	NP_001035233.1:p.Asn298Asp
NM_021007.2:c.892A>G	NP_066287.2:p.Asn298Asp
XM_005246750.2:c.892A>G	XP_005246807.1:p.Asn298Asp
XM_005246753.2:c.892A>G	XP_005246810.1:p.Asn298Asp
XM_005246754.3:c.862A>G	XP_005246811.1:p.Asn288Asp
XM_005246755.3:c.139A>G	XP_005246812.1:p.Asn47Asp
XM_011511608.1:c.892A>G	XP_011509910.1:p.Asn298Asp
XM_011511609.1:c.892A>G	XP_011509911.1:p.Asn298Asp
XM_005246753.3:c.892A>G	XP_005246810.1:p.Asn298Asp
XM_017004656.1:c.892A>G	XP_016860145.1:p.Asn298Asp
XM_017004657.1:c.892A>G	XP_016860146.1:p.Asn298Asp
XM_017004658.1:c.139A>G	XP_016860147.1:p.Asn47Asp
XM_024453037.1:c.139A>G	XP_024308805.1:p.Asn47Asp
NM_001040142.2:c.892A>G MANE Select	NP_001035232.1:p.Asn298Asp
NM_001040143.2:c.892A>G	NP_001035233.1:p.Asn298Asp
NM_001371246.1:c.892A>G MANE Plus Clinical	NP_001358175.1:p.Asn298Asp
NM_001371247.1:c.892A>G	NP_001358176.1:p.Asn298Asp
NM_021007.3:c.892A>G	NP_066287.2:p.Asn298Asp