Canonical Allele Identifier: CA349026013

Gene: SCN3A

Linked Data

• MyVariant Identifiers: chr2:g.165954010C>A (hg19) ; chr2:g.165097500C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165097500C>A , CM000664.2:g.165097500C>A	GRCh38
NC_000002.11:g.165954010C>A , CM000664.1:g.165954010C>A	GRCh37
NC_000002.10:g.165662256C>A	NCBI36
NG_042289.1:g.111589G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706067.1:c.3940G>T	ENSP00000516211.1:p.Ala1314Ser
ENST00000283254.12:c.3991G>T MANE Select	ENSP00000283254.7:p.Ala1331Ser
ENST00000638473.1:c.*1832G>T	ENSP00000491552.1:n.*1832G>T
ENST00000639244.1:c.3940G>T	ENSP00000492251.1:p.Ala1314Ser
ENST00000640652.1:c.*725G>T	ENSP00000492807.1:n.*725G>T
ENST00000658209.1:c.2200G>T	ENSP00000499598.1:n.2200G>T
ENST00000283254.11:c.3991G>T	ENSP00000283254.7:p.Ala1331Ser
ENST00000360093.7:c.3991G>T	ENSP00000353206.3:p.Ala1331Ser
ENST00000409101.7:c.3844G>T	ENSP00000386726.3:p.Ala1282Ser
ENST00000440431.6:c.3844G>T	ENSP00000403348.1:p.Ala1282Ser
ENST00000471697.1:n.115G>T
NM_001081676.1:c.3844G>T	NP_001075145.1:p.Ala1282Ser
NM_001081677.1:c.3844G>T	NP_001075146.1:p.Ala1282Ser
NM_006922.3:c.3991G>T	NP_008853.3:p.Ala1331Ser
XM_006712679.1:c.3991G>T	XP_006712742.1:p.Ala1331Ser
XM_011511610.1:c.3991G>T	XP_011509912.1:p.Ala1331Ser
XM_011511611.1:c.3991G>T	XP_011509913.1:p.Ala1331Ser
XM_011511612.1:c.3940G>T	XP_011509914.1:p.Ala1314Ser
XM_011511613.1:c.2101G>T	XP_011509915.1:p.Ala701Ser
XM_011511610.3:c.3991G>T	XP_011509912.1:p.Ala1331Ser
XM_011511613.3:c.2101G>T	XP_011509915.1:p.Ala701Ser
XM_017004660.2:c.3991G>T	XP_016860149.1:p.Ala1331Ser
XM_017004661.2:c.3940G>T	XP_016860150.1:p.Ala1314Ser
XM_017004662.2:c.3853G>T	XP_016860151.1:p.Ala1285Ser
XM_017004663.2:c.2101G>T	XP_016860152.1:p.Ala701Ser
NM_006922.4:c.3991G>T MANE Select	NP_008853.3:p.Ala1331Ser
NM_001081676.2:c.3844G>T	NP_001075145.1:p.Ala1282Ser
NM_001081677.2:c.3844G>T	NP_001075146.1:p.Ala1282Ser