Canonical Allele Identifier: CA1358640589

Gene: SCN10A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38725271G= , CM000665.2:g.38725271G=	GRCh38
NC_000003.11:g.38766762G= , CM000665.1:g.38766762G=	GRCh37
NC_000003.10:g.38741766G=	NCBI36
NG_031891.2:g.73740C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449082.3:c.3131C= MANE Select	ENSP00000390600.2:p.Thr1044=
ENST00000643924.1:c.3128C=	ENSP00000495595.1:p.Thr1043=
ENST00000655275.1:c.3155C=	ENSP00000499510.1:p.Thr1052=
ENST00000449082.2:c.3131C=	ENSP00000390600.2:p.Thr1044=
NM_001293306.2:c.3128C=	NP_001280235.2:p.Thr1043=
NM_001293307.2:c.2837C=	NP_001280236.2:p.Thr946=
NM_006514.3:c.3131C=	NP_006505.3:p.Thr1044=
XM_005265371.2:c.3140C=	XP_005265428.1:p.Thr1047=
XM_011533993.1:c.3137C=	XP_011532295.1:p.Thr1046=
XM_011533994.1:c.2846C=	XP_011532296.1:p.Thr949=
XM_005265371.3:c.3140C=	XP_005265428.1:p.Thr1047=
XM_011533993.2:c.3137C=	XP_011532295.1:p.Thr1046=
XM_011533994.2:c.2846C=	XP_011532296.1:p.Thr949=
NM_006514.4:c.3131C= MANE Select	NP_006505.4:p.Thr1044=