Canonical Allele Identifier: CA349024901

Gene: SCN3A

Linked Data

• MyVariant Identifiers: chr2:g.165953787G>A (hg19) ; chr2:g.165097277G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165097277G>A , CM000664.2:g.165097277G>A	GRCh38
NC_000002.11:g.165953787G>A , CM000664.1:g.165953787G>A	GRCh37
NC_000002.10:g.165662033G>A	NCBI36
NG_042289.1:g.111812C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000706067.1:c.4163C>T	ENSP00000516211.1:p.Ala1388Val
ENST00000283254.12:c.4214C>T MANE Select	ENSP00000283254.7:p.Ala1405Val
ENST00000638473.1:c.*2055C>T	ENSP00000491552.1:n.*2055C>T
ENST00000639244.1:c.4163C>T	ENSP00000492251.1:p.Ala1388Val
ENST00000640652.1:c.*948C>T	ENSP00000492807.1:n.*948C>T
ENST00000658209.1:c.2423C>T	ENSP00000499598.1:n.2423C>T
ENST00000283254.11:c.4214C>T	ENSP00000283254.7:p.Ala1405Val
ENST00000360093.7:c.4214C>T	ENSP00000353206.3:p.Ala1405Val
ENST00000409101.7:c.4067C>T	ENSP00000386726.3:p.Ala1356Val
ENST00000440431.6:c.4067C>T	ENSP00000403348.1:p.Ala1356Val
ENST00000471697.1:n.338C>T
NM_001081676.1:c.4067C>T	NP_001075145.1:p.Ala1356Val
NM_001081677.1:c.4067C>T	NP_001075146.1:p.Ala1356Val
NM_006922.3:c.4214C>T	NP_008853.3:p.Ala1405Val
XM_006712679.1:c.4214C>T	XP_006712742.1:p.Ala1405Val
XM_011511610.1:c.4214C>T	XP_011509912.1:p.Ala1405Val
XM_011511611.1:c.4214C>T	XP_011509913.1:p.Ala1405Val
XM_011511612.1:c.4163C>T	XP_011509914.1:p.Ala1388Val
XM_011511613.1:c.2324C>T	XP_011509915.1:p.Ala775Val
XM_011511610.3:c.4214C>T	XP_011509912.1:p.Ala1405Val
XM_011511613.3:c.2324C>T	XP_011509915.1:p.Ala775Val
XM_017004660.2:c.4214C>T	XP_016860149.1:p.Ala1405Val
XM_017004661.2:c.4163C>T	XP_016860150.1:p.Ala1388Val
XM_017004662.2:c.4076C>T	XP_016860151.1:p.Ala1359Val
XM_017004663.2:c.2324C>T	XP_016860152.1:p.Ala775Val
NM_006922.4:c.4214C>T MANE Select	NP_008853.3:p.Ala1405Val
NM_001081676.2:c.4067C>T	NP_001075145.1:p.Ala1356Val
NM_001081677.2:c.4067C>T	NP_001075146.1:p.Ala1356Val