Canonical Allele Identifier: CA1304438489

Gene: SCN3A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165097494G= , CM000664.2:g.165097494G=	GRCh38
NC_000002.11:g.165954004G= , CM000664.1:g.165954004G=	GRCh37
NC_000002.10:g.165662250G=	NCBI36
NG_042289.1:g.111595C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706067.1:c.3946C=	ENSP00000516211.1:p.Pro1316=
ENST00000283254.12:c.3997C= MANE Select	ENSP00000283254.7:p.Pro1333=
ENST00000638473.1:c.*1838C=	ENSP00000491552.1:n.*1838C=
ENST00000639244.1:c.3946C=	ENSP00000492251.1:p.Pro1316=
ENST00000640652.1:c.*731C=	ENSP00000492807.1:n.*731C=
ENST00000658209.1:c.2206C=	ENSP00000499598.1:n.2206C=
ENST00000283254.11:c.3997C=	ENSP00000283254.7:p.Pro1333=
ENST00000360093.7:c.3997C=	ENSP00000353206.3:p.Pro1333=
ENST00000409101.7:c.3850C=	ENSP00000386726.3:p.Pro1284=
ENST00000440431.6:c.3850C=	ENSP00000403348.1:p.Pro1284=
ENST00000471697.1:n.121C=
NM_001081676.1:c.3850C=	NP_001075145.1:p.Pro1284=
NM_001081677.1:c.3850C=	NP_001075146.1:p.Pro1284=
NM_006922.3:c.3997C=	NP_008853.3:p.Pro1333=
XM_006712679.1:c.3997C=	XP_006712742.1:p.Pro1333=
XM_011511610.1:c.3997C=	XP_011509912.1:p.Pro1333=
XM_011511611.1:c.3997C=	XP_011509913.1:p.Pro1333=
XM_011511612.1:c.3946C=	XP_011509914.1:p.Pro1316=
XM_011511613.1:c.2107C=	XP_011509915.1:p.Pro703=
XM_011511610.3:c.3997C=	XP_011509912.1:p.Pro1333=
XM_011511613.3:c.2107C=	XP_011509915.1:p.Pro703=
XM_017004660.2:c.3997C=	XP_016860149.1:p.Pro1333=
XM_017004661.2:c.3946C=	XP_016860150.1:p.Pro1316=
XM_017004662.2:c.3859C=	XP_016860151.1:p.Pro1287=
XM_017004663.2:c.2107C=	XP_016860152.1:p.Pro703=
NM_006922.4:c.3997C= MANE Select	NP_008853.3:p.Pro1333=
NM_001081676.2:c.3850C=	NP_001075145.1:p.Pro1284=
NM_001081677.2:c.3850C=	NP_001075146.1:p.Pro1284=