Canonical Allele Identifier: CA429885379

Gene: SCN2A

Linked Data

• MyVariant Identifiers: chr2:g.166201136G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165344626G>T , CM000664.2:g.165344626G>T	GRCh38
NC_000002.11:g.166201136G>T , CM000664.1:g.166201136G>T	GRCh37
NC_000002.10:g.165909382G>T	NCBI36
NG_008143.1:g.110225G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000631182.3:c.2634G>T MANE Plus Clinical	ENSP00000486885.1:p.Val878=
ENST00000375437.7:c.2634G>T MANE Select	ENSP00000364586.2:p.Val878=
ENST00000636071.2:c.2634G>T	ENSP00000490107.1:p.Val878=
ENST00000636135.1:c.*953G>T	ENSP00000489821.1:n.*953G>T
ENST00000636384.2:c.*621G>T	ENSP00000490765.1:n.*621G>T
ENST00000636662.2:c.*3157G>T	ENSP00000489873.1:n.*3157G>T
ENST00000636769.1:c.*576G>T	ENSP00000490800.1:n.*576G>T
ENST00000636985.2:c.2238G>T	ENSP00000490849.1:p.Val746=
ENST00000637266.2:c.2634G>T	ENSP00000490866.1:p.Val878=
ENST00000673831.1:c.72G>T	ENSP00000501305.1:p.Val24=
ENST00000673883.1:c.72G>T	ENSP00000501309.1:p.Val24=
ENST00000674133.1:c.485G>T
ENST00000283256.10:c.2634G>T	ENSP00000283256.6:p.Val878=
ENST00000375427.4:c.2634G>T	ENSP00000364576.2:p.Val878=
ENST00000375437.6:c.2634G>T	ENSP00000364586.2:p.Val878=
ENST00000480032.4:n.2777G>T
ENST00000631182.2:c.2634G>T	ENSP00000486885.1:p.Val878=
NM_001040142.1:c.2634G>T	NP_001035232.1:p.Val878=
NM_001040143.1:c.2634G>T	NP_001035233.1:p.Val878=
NM_021007.2:c.2634G>T	NP_066287.2:p.Val878=
XM_005246750.2:c.2634G>T	XP_005246807.1:p.Val878=
XM_005246753.2:c.2634G>T	XP_005246810.1:p.Val878=
XM_005246754.3:c.2604G>T	XP_005246811.1:p.Val868=
XM_005246755.3:c.1881G>T	XP_005246812.1:p.Val627=
XM_011511608.1:c.2634G>T	XP_011509910.1:p.Val878=
XM_011511609.1:c.2634G>T	XP_011509911.1:p.Val878=
XM_005246753.3:c.2634G>T	XP_005246810.1:p.Val878=
XM_017004656.1:c.2634G>T	XP_016860145.1:p.Val878=
XM_017004657.1:c.2634G>T	XP_016860146.1:p.Val878=
XM_017004658.1:c.1881G>T	XP_016860147.1:p.Val627=
XM_017004659.1:c.432G>T	XP_016860148.1:p.Val144=
XM_024453037.1:c.1881G>T	XP_024308805.1:p.Val627=
NM_001040142.2:c.2634G>T MANE Select	NP_001035232.1:p.Val878=
NM_001040143.2:c.2634G>T	NP_001035233.1:p.Val878=
NM_001371246.1:c.2634G>T MANE Plus Clinical	NP_001358175.1:p.Val878=
NM_001371247.1:c.2634G>T	NP_001358176.1:p.Val878=
NM_021007.3:c.2634G>T	NP_066287.2:p.Val878=