Canonical Allele Identifier: CA1358640592

Gene: SCN10A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38725274A= , CM000665.2:g.38725274A=	GRCh38
NC_000003.11:g.38766765A= , CM000665.1:g.38766765A=	GRCh37
NC_000003.10:g.38741769A=	NCBI36
NG_031891.2:g.73737T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449082.3:c.3128T= MANE Select	ENSP00000390600.2:p.Leu1043=
ENST00000643924.1:c.3125T=	ENSP00000495595.1:p.Leu1042=
ENST00000655275.1:c.3152T=	ENSP00000499510.1:p.Leu1051=
ENST00000449082.2:c.3128T=	ENSP00000390600.2:p.Leu1043=
NM_001293306.2:c.3125T=	NP_001280235.2:p.Leu1042=
NM_001293307.2:c.2834T=	NP_001280236.2:p.Leu945=
NM_006514.3:c.3128T=	NP_006505.3:p.Leu1043=
XM_005265371.2:c.3137T=	XP_005265428.1:p.Leu1046=
XM_011533993.1:c.3134T=	XP_011532295.1:p.Leu1045=
XM_011533994.1:c.2843T=	XP_011532296.1:p.Leu948=
XM_005265371.3:c.3137T=	XP_005265428.1:p.Leu1046=
XM_011533993.2:c.3134T=	XP_011532295.1:p.Leu1045=
XM_011533994.2:c.2843T=	XP_011532296.1:p.Leu948=
NM_006514.4:c.3128T= MANE Select	NP_006505.4:p.Leu1043=