Canonical Allele Identifier: CA2661741103

Gene: SCN2A

Linked Data

• gnomAD v4: 2-165377548-TAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165377551_165377552del , CM000664.2:g.165377551_165377552del	GRCh38
NC_000002.11:g.166234061_166234062del , CM000664.1:g.166234061_166234062del	GRCh37
NC_000002.10:g.165942307_165942308del	NCBI36
NG_008143.1:g.143150_143151del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000631182.3:c.4255-46_4255-45del MANE Plus Clinical	ENSP00000486885.1:n.4255-46_4255-45del
ENST00000375437.7:c.4255-46_4255-45del MANE Select	ENSP00000364586.2:n.4255-46_4255-45del
ENST00000636071.2:c.4255-46_4255-45del	ENSP00000490107.1:n.4255-46_4255-45del
ENST00000636135.1:c.*2574-46_*2574-45del	ENSP00000489821.1:n.*2574-46_*2574-45del
ENST00000636384.2:c.*2242-46_*2242-45del	ENSP00000490765.1:n.*2242-46_*2242-45del
ENST00000636662.2:c.*4778-46_*4778-45del	ENSP00000489873.1:n.*4778-46_*4778-45del
ENST00000636769.1:c.*2197-46_*2197-45del	ENSP00000490800.1:n.*2197-46_*2197-45del
ENST00000636985.2:c.3859-46_3859-45del	ENSP00000490849.1:n.3859-46_3859-45del
ENST00000637266.2:c.4255-46_4255-45del	ENSP00000490866.1:n.4255-46_4255-45del
ENST00000283256.10:c.4255-46_4255-45del	ENSP00000283256.6:n.4255-46_4255-45del
ENST00000375427.4:c.4255-46_4255-45del	ENSP00000364576.2:n.4255-46_4255-45del
ENST00000375437.6:c.4255-46_4255-45del	ENSP00000364586.2:n.4255-46_4255-45del
ENST00000480032.4:n.7323-46_7323-45del
ENST00000631182.2:c.4255-46_4255-45del	ENSP00000486885.1:n.4255-46_4255-45del
NM_001040142.1:c.4255-46_4255-45del	NP_001035232.1:n.4255-46_4255-45del
NM_001040143.1:c.4255-46_4255-45del	NP_001035233.1:n.4255-46_4255-45del
NM_021007.2:c.4255-46_4255-45del	NP_066287.2:n.4255-46_4255-45del
XM_005246750.2:c.4255-46_4255-45del	XP_005246807.1:n.4255-46_4255-45del
XM_005246753.2:c.4255-46_4255-45del	XP_005246810.1:n.4255-46_4255-45del
XM_005246754.3:c.4225-46_4225-45del	XP_005246811.1:n.4225-46_4225-45del
XM_005246755.3:c.3502-46_3502-45del	XP_005246812.1:n.3502-46_3502-45del
XM_011511608.1:c.4255-46_4255-45del	XP_011509910.1:n.4255-46_4255-45del
XM_011511609.1:c.4255-46_4255-45del	XP_011509911.1:n.4255-46_4255-45del
XM_005246753.3:c.4255-46_4255-45del	XP_005246810.1:n.4255-46_4255-45del
XM_017004656.1:c.4255-46_4255-45del	XP_016860145.1:n.4255-46_4255-45del
XM_017004657.1:c.4255-46_4255-45del	XP_016860146.1:n.4255-46_4255-45del
XM_017004658.1:c.3502-46_3502-45del	XP_016860147.1:n.3502-46_3502-45del
XM_017004659.1:c.2053-46_2053-45del	XP_016860148.1:n.2053-46_2053-45del
XM_024453037.1:c.3502-46_3502-45del	XP_024308805.1:n.3502-46_3502-45del
NM_001040142.2:c.4255-46_4255-45del MANE Select	NP_001035232.1:n.4255-46_4255-45del
NM_001040143.2:c.4255-46_4255-45del	NP_001035233.1:n.4255-46_4255-45del
NM_001371246.1:c.4255-46_4255-45del MANE Plus Clinical	NP_001358175.1:n.4255-46_4255-45del
NM_001371247.1:c.4255-46_4255-45del	NP_001358176.1:n.4255-46_4255-45del
NM_021007.3:c.4255-46_4255-45del	NP_066287.2:n.4255-46_4255-45del