Canonical Allele Identifier: CA1358640556

Gene: SCN10A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38725188G= , CM000665.2:g.38725188G=	GRCh38
NC_000003.11:g.38766679G= , CM000665.1:g.38766679G=	GRCh37
NC_000003.10:g.38741683G=	NCBI36
NG_031891.2:g.73823C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449082.3:c.3214C= MANE Select	ENSP00000390600.2:p.Gln1072=
ENST00000643924.1:c.3211C=	ENSP00000495595.1:p.Gln1071=
ENST00000655275.1:c.3238C=	ENSP00000499510.1:p.Gln1080=
ENST00000449082.2:c.3214C=	ENSP00000390600.2:p.Gln1072=
NM_001293306.2:c.3211C=	NP_001280235.2:p.Gln1071=
NM_001293307.2:c.2920C=	NP_001280236.2:p.Gln974=
NM_006514.3:c.3214C=	NP_006505.3:p.Gln1072=
XM_005265371.2:c.3223C=	XP_005265428.1:p.Gln1075=
XM_011533993.1:c.3220C=	XP_011532295.1:p.Gln1074=
XM_011533994.1:c.2929C=	XP_011532296.1:p.Gln977=
XM_005265371.3:c.3223C=	XP_005265428.1:p.Gln1075=
XM_011533993.2:c.3220C=	XP_011532295.1:p.Gln1074=
XM_011533994.2:c.2929C=	XP_011532296.1:p.Gln977=
NM_006514.4:c.3214C= MANE Select	NP_006505.4:p.Gln1072=