Canonical Allele Identifier: CA1358640604

Gene: SCN10A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38725294G= , CM000665.2:g.38725294G=	GRCh38
NC_000003.11:g.38766785G= , CM000665.1:g.38766785G=	GRCh37
NC_000003.10:g.38741789G=	NCBI36
NG_031891.2:g.73717C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449082.3:c.3108C= MANE Select	ENSP00000390600.2:p.Val1036=
ENST00000643924.1:c.3105C=	ENSP00000495595.1:p.Val1035=
ENST00000655275.1:c.3132C=	ENSP00000499510.1:p.Val1044=
ENST00000449082.2:c.3108C=	ENSP00000390600.2:p.Val1036=
NM_001293306.2:c.3105C=	NP_001280235.2:p.Val1035=
NM_001293307.2:c.2814C=	NP_001280236.2:p.Val938=
NM_006514.3:c.3108C=	NP_006505.3:p.Val1036=
XM_005265371.2:c.3117C=	XP_005265428.1:p.Val1039=
XM_011533993.1:c.3114C=	XP_011532295.1:p.Val1038=
XM_011533994.1:c.2823C=	XP_011532296.1:p.Val941=
XM_005265371.3:c.3117C=	XP_005265428.1:p.Val1039=
XM_011533993.2:c.3114C=	XP_011532295.1:p.Val1038=
XM_011533994.2:c.2823C=	XP_011532296.1:p.Val941=
NM_006514.4:c.3108C= MANE Select	NP_006505.4:p.Val1036=