Canonical Allele Identifier: CA1358640563

Gene: SCN10A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38725214T= , CM000665.2:g.38725214T=	GRCh38
NC_000003.11:g.38766705T= , CM000665.1:g.38766705T=	GRCh37
NC_000003.10:g.38741709T=	NCBI36
NG_031891.2:g.73797A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449082.3:c.3188A= MANE Select	ENSP00000390600.2:p.Glu1063=
ENST00000643924.1:c.3185A=	ENSP00000495595.1:p.Glu1062=
ENST00000655275.1:c.3212A=	ENSP00000499510.1:p.Glu1071=
ENST00000449082.2:c.3188A=	ENSP00000390600.2:p.Glu1063=
NM_001293306.2:c.3185A=	NP_001280235.2:p.Glu1062=
NM_001293307.2:c.2894A=	NP_001280236.2:p.Glu965=
NM_006514.3:c.3188A=	NP_006505.3:p.Glu1063=
XM_005265371.2:c.3197A=	XP_005265428.1:p.Glu1066=
XM_011533993.1:c.3194A=	XP_011532295.1:p.Glu1065=
XM_011533994.1:c.2903A=	XP_011532296.1:p.Glu968=
XM_005265371.3:c.3197A=	XP_005265428.1:p.Glu1066=
XM_011533993.2:c.3194A=	XP_011532295.1:p.Glu1065=
XM_011533994.2:c.2903A=	XP_011532296.1:p.Glu968=
NM_006514.4:c.3188A= MANE Select	NP_006505.4:p.Glu1063=