Canonical Allele Identifier: CA349033428

Gene: SCN3A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165113856G>A , CM000664.2:g.165113856G>A	GRCh38
NC_000002.11:g.165970366G>A , CM000664.1:g.165970366G>A	GRCh37
NC_000002.10:g.165678612G>A	NCBI36
NG_042289.1:g.95233C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_006922.4:c.3629C>T MANE Select	NP_008853.3:p.Thr1210Ile
ENST00000283254.12:c.3629C>T MANE Select	ENSP00000283254.7:p.Thr1210Ile
NM_001081676.1:c.3482C>T	NP_001075145.1:p.Thr1161Ile
NM_001081676.2:c.3482C>T	NP_001075145.1:p.Thr1161Ile
NM_001081677.1:c.3482C>T	NP_001075146.1:p.Thr1161Ile
NM_001081677.2:c.3482C>T	NP_001075146.1:p.Thr1161Ile
NM_006922.3:c.3629C>T	NP_008853.3:p.Thr1210Ile
ENST00000283254.11:c.3629C>T	ENSP00000283254.7:p.Thr1210Ile
ENST00000360093.7:c.3629C>T	ENSP00000353206.3:p.Thr1210Ile
ENST00000409101.7:c.3482C>T	ENSP00000386726.3:p.Thr1161Ile
ENST00000440431.6:c.3482C>T	ENSP00000403348.1:p.Thr1161Ile
ENST00000638473.1:c.*1470C>T	ENSP00000491552.1:n.*1470C>T
ENST00000639244.1:c.3578C>T	ENSP00000492251.1:p.Thr1193Ile
ENST00000640652.1:c.*363C>T	ENSP00000492807.1:n.*363C>T
ENST00000658209.1:c.1838C>T	ENSP00000499598.1:n.1838C>T
ENST00000706067.1:c.3578C>T	ENSP00000516211.1:p.Thr1193Ile
XM_006712679.1:c.3629C>T	XP_006712742.1:p.Thr1210Ile
XM_011511610.1:c.3629C>T	XP_011509912.1:p.Thr1210Ile
XM_011511610.3:c.3629C>T	XP_011509912.1:p.Thr1210Ile
XM_011511611.1:c.3629C>T	XP_011509913.1:p.Thr1210Ile
XM_011511612.1:c.3578C>T	XP_011509914.1:p.Thr1193Ile
XM_011511613.1:c.1739C>T	XP_011509915.1:p.Thr580Ile
XM_011511613.3:c.1739C>T	XP_011509915.1:p.Thr580Ile
XM_017004660.2:c.3629C>T	XP_016860149.1:p.Thr1210Ile
XM_017004661.2:c.3578C>T	XP_016860150.1:p.Thr1193Ile
XM_017004662.2:c.3491C>T	XP_016860151.1:p.Thr1164Ile
XM_017004663.2:c.1739C>T	XP_016860152.1:p.Thr580Ile