Canonical Allele Identifier: CA2661736454

Gene: SCN2A

Linked Data

• gnomAD v4: 2-165308536-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165308539del , CM000664.2:g.165308539del	GRCh38
NC_000002.11:g.166165049del , CM000664.1:g.166165049del	GRCh37
NC_000002.10:g.165873295del	NCBI36
NG_008143.1:g.74138del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000631182.3:c.477-127del MANE Plus Clinical	ENSP00000486885.1:n.477-127del
ENST00000375437.7:c.477-127del MANE Select	ENSP00000364586.2:n.477-127del
ENST00000635945.1:n.840-127del
ENST00000636071.2:c.477-127del	ENSP00000490107.1:n.477-127del
ENST00000636135.1:c.476+602del	ENSP00000489821.1:n.476+602del
ENST00000636384.2:c.477-127del	ENSP00000490765.1:n.477-127del
ENST00000636662.2:c.*1000-127del	ENSP00000489873.1:n.*1000-127del
ENST00000636769.1:c.477-127del	ENSP00000490800.1:n.477-127del
ENST00000636985.2:c.81-127del	ENSP00000490849.1:n.81-127del
ENST00000637266.2:c.477-127del	ENSP00000490866.1:n.477-127del
ENST00000637367.1:c.*410-127del	ENSP00000490592.1:n.*410-127del
ENST00000638151.1:n.561-127del
ENST00000283256.10:c.477-127del	ENSP00000283256.6:n.477-127del
ENST00000375427.4:c.477-127del	ENSP00000364576.2:n.477-127del
ENST00000375437.6:c.477-127del	ENSP00000364586.2:n.477-127del
ENST00000424833.5:c.477-127del	ENSP00000406454.2:n.477-127del
ENST00000480032.4:n.620-127del
ENST00000486878.2:c.18-127del	ENSP00000487466.1:n.18-127del
ENST00000631182.2:c.477-127del	ENSP00000486885.1:n.477-127del
NM_001040142.1:c.477-127del	NP_001035232.1:n.477-127del
NM_001040143.1:c.477-127del	NP_001035233.1:n.477-127del
NM_021007.2:c.477-127del	NP_066287.2:n.477-127del
XM_005246750.2:c.477-127del	XP_005246807.1:n.477-127del
XM_005246753.2:c.477-127del	XP_005246810.1:n.477-127del
XM_005246754.3:c.447-127del	XP_005246811.1:n.447-127del
XM_011511608.1:c.477-127del	XP_011509910.1:n.477-127del
XM_011511609.1:c.477-127del	XP_011509911.1:n.477-127del
XM_005246753.3:c.477-127del	XP_005246810.1:n.477-127del
XM_017004656.1:c.477-127del	XP_016860145.1:n.477-127del
XM_017004657.1:c.477-127del	XP_016860146.1:n.477-127del
XM_017004658.1:c.-464-127del	XP_016860147.1:n.-464-127del
XM_024453037.1:c.-185-127del	XP_024308805.1:n.-185-127del
NM_001040142.2:c.477-127del MANE Select	NP_001035232.1:n.477-127del
NM_001040143.2:c.477-127del	NP_001035233.1:n.477-127del
NM_001371246.1:c.477-127del MANE Plus Clinical	NP_001358175.1:n.477-127del
NM_001371247.1:c.477-127del	NP_001358176.1:n.477-127del
NM_021007.3:c.477-127del	NP_066287.2:n.477-127del