Canonical Allele Identifier: CA1358640838

Gene: SCN10A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38725806G= , CM000665.2:g.38725806G=	GRCh38
NC_000003.11:g.38767297G= , CM000665.1:g.38767297G=	GRCh37
NC_000003.10:g.38742301G=	NCBI36
NG_031891.2:g.73205C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449082.3:c.3088-492C= MANE Select	ENSP00000390600.2:n.3088-492C=
ENST00000643924.1:c.3088-495C=	ENSP00000495595.1:n.3088-495C=
ENST00000655275.1:c.3115-495C=	ENSP00000499510.1:n.3115-495C=
ENST00000449082.2:c.3088-492C=	ENSP00000390600.2:n.3088-492C=
NM_001293306.2:c.3088-495C=	NP_001280235.2:n.3088-495C=
NM_001293307.2:c.2794-492C=	NP_001280236.2:n.2794-492C=
NM_006514.3:c.3088-492C=	NP_006505.3:n.3088-492C=
XM_005265371.2:c.3097-492C=	XP_005265428.1:n.3097-492C=
XM_011533993.1:c.3097-495C=	XP_011532295.1:n.3097-495C=
XM_011533994.1:c.2803-492C=	XP_011532296.1:n.2803-492C=
XM_005265371.3:c.3097-492C=	XP_005265428.1:n.3097-492C=
XM_011533993.2:c.3097-495C=	XP_011532295.1:n.3097-495C=
XM_011533994.2:c.2803-492C=	XP_011532296.1:n.2803-492C=
NM_006514.4:c.3088-492C= MANE Select	NP_006505.4:n.3088-492C=