Canonical Allele Identifier: CA1358640587

Gene: SCN10A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38725266T= , CM000665.2:g.38725266T=	GRCh38
NC_000003.11:g.38766757T= , CM000665.1:g.38766757T=	GRCh37
NC_000003.10:g.38741761T=	NCBI36
NG_031891.2:g.73745A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449082.3:c.3136A= MANE Select	ENSP00000390600.2:p.Arg1046=
ENST00000643924.1:c.3133A=	ENSP00000495595.1:p.Arg1045=
ENST00000655275.1:c.3160A=	ENSP00000499510.1:p.Arg1054=
ENST00000449082.2:c.3136A=	ENSP00000390600.2:p.Arg1046=
NM_001293306.2:c.3133A=	NP_001280235.2:p.Arg1045=
NM_001293307.2:c.2842A=	NP_001280236.2:p.Arg948=
NM_006514.3:c.3136A=	NP_006505.3:p.Arg1046=
XM_005265371.2:c.3145A=	XP_005265428.1:p.Arg1049=
XM_011533993.1:c.3142A=	XP_011532295.1:p.Arg1048=
XM_011533994.1:c.2851A=	XP_011532296.1:p.Arg951=
XM_005265371.3:c.3145A=	XP_005265428.1:p.Arg1049=
XM_011533993.2:c.3142A=	XP_011532295.1:p.Arg1048=
XM_011533994.2:c.2851A=	XP_011532296.1:p.Arg951=
NM_006514.4:c.3136A= MANE Select	NP_006505.4:p.Arg1046=