Canonical Allele Identifier: CA1304438491

Gene: SCN3A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165097498T= , CM000664.2:g.165097498T=	GRCh38
NC_000002.11:g.165954008T= , CM000664.1:g.165954008T=	GRCh37
NC_000002.10:g.165662254T=	NCBI36
NG_042289.1:g.111591A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706067.1:c.3942A=	ENSP00000516211.1:p.Ala1314=
ENST00000283254.12:c.3993A= MANE Select	ENSP00000283254.7:p.Ala1331=
ENST00000638473.1:c.*1834A=	ENSP00000491552.1:n.*1834A=
ENST00000639244.1:c.3942A=	ENSP00000492251.1:p.Ala1314=
ENST00000640652.1:c.*727A=	ENSP00000492807.1:n.*727A=
ENST00000658209.1:c.2202A=	ENSP00000499598.1:n.2202A=
ENST00000283254.11:c.3993A=	ENSP00000283254.7:p.Ala1331=
ENST00000360093.7:c.3993A=	ENSP00000353206.3:p.Ala1331=
ENST00000409101.7:c.3846A=	ENSP00000386726.3:p.Ala1282=
ENST00000440431.6:c.3846A=	ENSP00000403348.1:p.Ala1282=
ENST00000471697.1:n.117A=
NM_001081676.1:c.3846A=	NP_001075145.1:p.Ala1282=
NM_001081677.1:c.3846A=	NP_001075146.1:p.Ala1282=
NM_006922.3:c.3993A=	NP_008853.3:p.Ala1331=
XM_006712679.1:c.3993A=	XP_006712742.1:p.Ala1331=
XM_011511610.1:c.3993A=	XP_011509912.1:p.Ala1331=
XM_011511611.1:c.3993A=	XP_011509913.1:p.Ala1331=
XM_011511612.1:c.3942A=	XP_011509914.1:p.Ala1314=
XM_011511613.1:c.2103A=	XP_011509915.1:p.Ala701=
XM_011511610.3:c.3993A=	XP_011509912.1:p.Ala1331=
XM_011511613.3:c.2103A=	XP_011509915.1:p.Ala701=
XM_017004660.2:c.3993A=	XP_016860149.1:p.Ala1331=
XM_017004661.2:c.3942A=	XP_016860150.1:p.Ala1314=
XM_017004662.2:c.3855A=	XP_016860151.1:p.Ala1285=
XM_017004663.2:c.2103A=	XP_016860152.1:p.Ala701=
NM_006922.4:c.3993A= MANE Select	NP_008853.3:p.Ala1331=
NM_001081676.2:c.3846A=	NP_001075145.1:p.Ala1282=
NM_001081677.2:c.3846A=	NP_001075146.1:p.Ala1282=