Canonical Allele Identifier: CA349025395
Gene: SCN3A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.165097334G>A , CM000664.2:g.165097334G>A GRCh38
NC_000002.11:g.165953844G>A , CM000664.1:g.165953844G>A GRCh37
NC_000002.10:g.165662090G>A NCBI36
NG_042289.1:g.111755C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000706067.1:c.4106C>T ENSP00000516211.1:p.Ala1369Val
ENST00000283254.12:c.4157C>T MANE Select ENSP00000283254.7:p.Ala1386Val
ENST00000638473.1:c.*1998C>T ENSP00000491552.1:n.*1998C>T
ENST00000639244.1:c.4106C>T ENSP00000492251.1:p.Ala1369Val
ENST00000640652.1:c.*891C>T ENSP00000492807.1:n.*891C>T
ENST00000658209.1:c.2366C>T ENSP00000499598.1:n.2366C>T
ENST00000283254.11:c.4157C>T ENSP00000283254.7:p.Ala1386Val
ENST00000360093.7:c.4157C>T ENSP00000353206.3:p.Ala1386Val
ENST00000409101.7:c.4010C>T ENSP00000386726.3:p.Ala1337Val
ENST00000440431.6:c.4010C>T ENSP00000403348.1:p.Ala1337Val
ENST00000471697.1:n.281C>T
NM_001081676.1:c.4010C>T NP_001075145.1:p.Ala1337Val
NM_001081677.1:c.4010C>T NP_001075146.1:p.Ala1337Val
NM_006922.3:c.4157C>T NP_008853.3:p.Ala1386Val
XM_006712679.1:c.4157C>T XP_006712742.1:p.Ala1386Val
XM_011511610.1:c.4157C>T XP_011509912.1:p.Ala1386Val
XM_011511611.1:c.4157C>T XP_011509913.1:p.Ala1386Val
XM_011511612.1:c.4106C>T XP_011509914.1:p.Ala1369Val
XM_011511613.1:c.2267C>T XP_011509915.1:p.Ala756Val
XM_011511610.3:c.4157C>T XP_011509912.1:p.Ala1386Val
XM_011511613.3:c.2267C>T XP_011509915.1:p.Ala756Val
XM_017004660.2:c.4157C>T XP_016860149.1:p.Ala1386Val
XM_017004661.2:c.4106C>T XP_016860150.1:p.Ala1369Val
XM_017004662.2:c.4019C>T XP_016860151.1:p.Ala1340Val
XM_017004663.2:c.2267C>T XP_016860152.1:p.Ala756Val
NM_006922.4:c.4157C>T MANE Select NP_008853.3:p.Ala1386Val
NM_001081676.2:c.4010C>T NP_001075145.1:p.Ala1337Val
NM_001081677.2:c.4010C>T NP_001075146.1:p.Ala1337Val