Canonical Allele Identifier: CA1358639760

Gene: SCN10A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38723527C= , CM000665.2:g.38723527C=	GRCh38
NC_000003.11:g.38765018C= , CM000665.1:g.38765018C=	GRCh37
NC_000003.10:g.38740022C=	NCBI36
NG_031891.2:g.75484G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449082.3:c.3255G= MANE Select	ENSP00000390600.2:p.Glu1085=
ENST00000643924.1:c.3252G=	ENSP00000495595.1:p.Glu1084=
ENST00000655275.1:c.3279G=	ENSP00000499510.1:p.Glu1093=
ENST00000449082.2:c.3255G=	ENSP00000390600.2:p.Glu1085=
NM_001293306.2:c.3252G=	NP_001280235.2:p.Glu1084=
NM_001293307.2:c.2961G=	NP_001280236.2:p.Glu987=
NM_006514.3:c.3255G=	NP_006505.3:p.Glu1085=
XM_005265371.2:c.3264G=	XP_005265428.1:p.Glu1088=
XM_011533993.1:c.3261G=	XP_011532295.1:p.Glu1087=
XM_011533994.1:c.2970G=	XP_011532296.1:p.Glu990=
XM_005265371.3:c.3264G=	XP_005265428.1:p.Glu1088=
XM_011533993.2:c.3261G=	XP_011532295.1:p.Glu1087=
XM_011533994.2:c.2970G=	XP_011532296.1:p.Glu990=
NM_006514.4:c.3255G= MANE Select	NP_006505.4:p.Glu1085=