Canonical Allele Identifier: CA1358640585

Gene: SCN10A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38725263T= , CM000665.2:g.38725263T=	GRCh38
NC_000003.11:g.38766754T= , CM000665.1:g.38766754T=	GRCh37
NC_000003.10:g.38741758T=	NCBI36
NG_031891.2:g.73748A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449082.3:c.3139A= MANE Select	ENSP00000390600.2:p.Ser1047=
ENST00000643924.1:c.3136A=	ENSP00000495595.1:p.Ser1046=
ENST00000655275.1:c.3163A=	ENSP00000499510.1:p.Ser1055=
ENST00000449082.2:c.3139A=	ENSP00000390600.2:p.Ser1047=
NM_001293306.2:c.3136A=	NP_001280235.2:p.Ser1046=
NM_001293307.2:c.2845A=	NP_001280236.2:p.Ser949=
NM_006514.3:c.3139A=	NP_006505.3:p.Ser1047=
XM_005265371.2:c.3148A=	XP_005265428.1:p.Ser1050=
XM_011533993.1:c.3145A=	XP_011532295.1:p.Ser1049=
XM_011533994.1:c.2854A=	XP_011532296.1:p.Ser952=
XM_005265371.3:c.3148A=	XP_005265428.1:p.Ser1050=
XM_011533993.2:c.3145A=	XP_011532295.1:p.Ser1049=
XM_011533994.2:c.2854A=	XP_011532296.1:p.Ser952=
NM_006514.4:c.3139A= MANE Select	NP_006505.4:p.Ser1047=