Canonical Allele Identifier: CA1304438548

Gene: SCN3A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165097621A= , CM000664.2:g.165097621A=	GRCh38
NC_000002.11:g.165954131A= , CM000664.1:g.165954131A=	GRCh37
NC_000002.10:g.165662377A=	NCBI36
NG_042289.1:g.111468T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706067.1:c.3916-97T=	ENSP00000516211.1:n.3916-97T=
ENST00000283254.12:c.3967-97T= MANE Select	ENSP00000283254.7:n.3967-97T=
ENST00000638473.1:c.*1808-97T=	ENSP00000491552.1:n.*1808-97T=
ENST00000639244.1:c.3916-97T=	ENSP00000492251.1:n.3916-97T=
ENST00000640652.1:c.*701-97T=	ENSP00000492807.1:n.*701-97T=
ENST00000658209.1:c.2176-97T=	ENSP00000499598.1:n.2176-97T=
ENST00000283254.11:c.3967-97T=	ENSP00000283254.7:n.3967-97T=
ENST00000360093.7:c.3967-97T=	ENSP00000353206.3:n.3967-97T=
ENST00000409101.7:c.3820-97T=	ENSP00000386726.3:n.3820-97T=
ENST00000440431.6:c.3820-97T=	ENSP00000403348.1:n.3820-97T=
NM_001081676.1:c.3820-97T=	NP_001075145.1:n.3820-97T=
NM_001081677.1:c.3820-97T=	NP_001075146.1:n.3820-97T=
NM_006922.3:c.3967-97T=	NP_008853.3:n.3967-97T=
XM_006712679.1:c.3967-97T=	XP_006712742.1:n.3967-97T=
XM_011511610.1:c.3967-97T=	XP_011509912.1:n.3967-97T=
XM_011511611.1:c.3967-97T=	XP_011509913.1:n.3967-97T=
XM_011511612.1:c.3916-97T=	XP_011509914.1:n.3916-97T=
XM_011511613.1:c.2077-97T=	XP_011509915.1:n.2077-97T=
XM_011511610.3:c.3967-97T=	XP_011509912.1:n.3967-97T=
XM_011511613.3:c.2077-97T=	XP_011509915.1:n.2077-97T=
XM_017004660.2:c.3967-97T=	XP_016860149.1:n.3967-97T=
XM_017004661.2:c.3916-97T=	XP_016860150.1:n.3916-97T=
XM_017004662.2:c.3829-97T=	XP_016860151.1:n.3829-97T=
XM_017004663.2:c.2077-97T=	XP_016860152.1:n.2077-97T=
NM_006922.4:c.3967-97T= MANE Select	NP_008853.3:n.3967-97T=
NM_001081676.2:c.3820-97T=	NP_001075145.1:n.3820-97T=
NM_001081677.2:c.3820-97T=	NP_001075146.1:n.3820-97T=