Canonical Allele Identifier: CA1358653200

Gene: SCN10A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38752234T= , CM000665.2:g.38752234T=	GRCh38
NC_000003.11:g.38793725T= , CM000665.1:g.38793725T=	GRCh37
NC_000003.10:g.38768729T=	NCBI36
NG_031891.2:g.46777A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000449082.3:c.1740A= MANE Select	ENSP00000390600.2:p.Gly580=
ENST00000643924.1:c.1740A=	ENSP00000495595.1:p.Gly580=
ENST00000655275.1:c.1767A=	ENSP00000499510.1:p.Gly589=
ENST00000449082.2:c.1740A=	ENSP00000390600.2:p.Gly580=
NM_001293306.2:c.1740A=	NP_001280235.2:p.Gly580=
NM_001293307.2:c.1462-2050A=	NP_001280236.2:n.1462-2050A=
NM_006514.3:c.1740A=	NP_006505.3:p.Gly580=
XM_005265371.2:c.1749A=	XP_005265428.1:p.Gly583=
XM_011533993.1:c.1749A=	XP_011532295.1:p.Gly583=
XM_011533994.1:c.1471-2050A=	XP_011532296.1:n.1471-2050A=
XM_005265371.3:c.1749A=	XP_005265428.1:p.Gly583=
XM_011533993.2:c.1749A=	XP_011532295.1:p.Gly583=
XM_011533994.2:c.1471-2050A=	XP_011532296.1:n.1471-2050A=
NM_006514.4:c.1740A= MANE Select	NP_006505.4:p.Gly580=