Canonical Allele Identifier: CA1358640594

Gene: SCN10A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38725276G= , CM000665.2:g.38725276G=	GRCh38
NC_000003.11:g.38766767G= , CM000665.1:g.38766767G=	GRCh37
NC_000003.10:g.38741771G=	NCBI36
NG_031891.2:g.73735C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449082.3:c.3126C= MANE Select	ENSP00000390600.2:p.His1042=
ENST00000643924.1:c.3123C=	ENSP00000495595.1:p.His1041=
ENST00000655275.1:c.3150C=	ENSP00000499510.1:p.His1050=
ENST00000449082.2:c.3126C=	ENSP00000390600.2:p.His1042=
NM_001293306.2:c.3123C=	NP_001280235.2:p.His1041=
NM_001293307.2:c.2832C=	NP_001280236.2:p.His944=
NM_006514.3:c.3126C=	NP_006505.3:p.His1042=
XM_005265371.2:c.3135C=	XP_005265428.1:p.His1045=
XM_011533993.1:c.3132C=	XP_011532295.1:p.His1044=
XM_011533994.1:c.2841C=	XP_011532296.1:p.His947=
XM_005265371.3:c.3135C=	XP_005265428.1:p.His1045=
XM_011533993.2:c.3132C=	XP_011532295.1:p.His1044=
XM_011533994.2:c.2841C=	XP_011532296.1:p.His947=
NM_006514.4:c.3126C= MANE Select	NP_006505.4:p.His1042=