Canonical Allele Identifier: CA1358644173

Gene: SCN10A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38733341C= , CM000665.2:g.38733341C=	GRCh38
NC_000003.11:g.38774832C= , CM000665.1:g.38774832C=	GRCh37
NC_000003.10:g.38749836C=	NCBI36
NG_031891.2:g.65670G=

Transcript Alleles

HGVS	Amino-acid Change
NM_006514.4:c.2281-4440G= MANE Select	NP_006505.4:n.2281-4440G=
ENST00000449082.3:c.2281-4440G= MANE Select	ENSP00000390600.2:n.2281-4440G=
NM_001293306.2:c.2281-4440G=	NP_001280235.2:n.2281-4440G=
NM_001293307.2:c.1987-4440G=	NP_001280236.2:n.1987-4440G=
NM_006514.3:c.2281-4440G=	NP_006505.3:n.2281-4440G=
ENST00000449082.2:c.2281-4440G=	ENSP00000390600.2:n.2281-4440G=
ENST00000643924.1:c.2281-4440G=	ENSP00000495595.1:n.2281-4440G=
ENST00000655275.1:c.2308-4440G=	ENSP00000499510.1:n.2308-4440G=
XM_005265371.2:c.2290-4440G=	XP_005265428.1:n.2290-4440G=
XM_005265371.3:c.2290-4440G=	XP_005265428.1:n.2290-4440G=
XM_011533993.1:c.2290-4440G=	XP_011532295.1:n.2290-4440G=
XM_011533993.2:c.2290-4440G=	XP_011532295.1:n.2290-4440G=
XM_011533994.1:c.1996-4440G=	XP_011532296.1:n.1996-4440G=
XM_011533994.2:c.1996-4440G=	XP_011532296.1:n.1996-4440G=