Canonical Allele Identifier: CA1358640578

Gene: SCN10A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38725246T= , CM000665.2:g.38725246T=	GRCh38
NC_000003.11:g.38766737T= , CM000665.1:g.38766737T=	GRCh37
NC_000003.10:g.38741741T=	NCBI36
NG_031891.2:g.73765A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449082.3:c.3156A= MANE Select	ENSP00000390600.2:p.Thr1052=
ENST00000643924.1:c.3153A=	ENSP00000495595.1:p.Thr1051=
ENST00000655275.1:c.3180A=	ENSP00000499510.1:p.Thr1060=
ENST00000449082.2:c.3156A=	ENSP00000390600.2:p.Thr1052=
NM_001293306.2:c.3153A=	NP_001280235.2:p.Thr1051=
NM_001293307.2:c.2862A=	NP_001280236.2:p.Thr954=
NM_006514.3:c.3156A=	NP_006505.3:p.Thr1052=
XM_005265371.2:c.3165A=	XP_005265428.1:p.Thr1055=
XM_011533993.1:c.3162A=	XP_011532295.1:p.Thr1054=
XM_011533994.1:c.2871A=	XP_011532296.1:p.Thr957=
XM_005265371.3:c.3165A=	XP_005265428.1:p.Thr1055=
XM_011533993.2:c.3162A=	XP_011532295.1:p.Thr1054=
XM_011533994.2:c.2871A=	XP_011532296.1:p.Thr957=
NM_006514.4:c.3156A= MANE Select	NP_006505.4:p.Thr1052=