Canonical Allele Identifier: CA1358640600

Gene: SCN10A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38725286C= , CM000665.2:g.38725286C=	GRCh38
NC_000003.11:g.38766777C= , CM000665.1:g.38766777C=	GRCh37
NC_000003.10:g.38741781C=	NCBI36
NG_031891.2:g.73725G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449082.3:c.3116G= MANE Select	ENSP00000390600.2:p.Cys1039=
ENST00000643924.1:c.3113G=	ENSP00000495595.1:p.Cys1038=
ENST00000655275.1:c.3140G=	ENSP00000499510.1:p.Cys1047=
ENST00000449082.2:c.3116G=	ENSP00000390600.2:p.Cys1039=
NM_001293306.2:c.3113G=	NP_001280235.2:p.Cys1038=
NM_001293307.2:c.2822G=	NP_001280236.2:p.Cys941=
NM_006514.3:c.3116G=	NP_006505.3:p.Cys1039=
XM_005265371.2:c.3125G=	XP_005265428.1:p.Cys1042=
XM_011533993.1:c.3122G=	XP_011532295.1:p.Cys1041=
XM_011533994.1:c.2831G=	XP_011532296.1:p.Cys944=
XM_005265371.3:c.3125G=	XP_005265428.1:p.Cys1042=
XM_011533993.2:c.3122G=	XP_011532295.1:p.Cys1041=
XM_011533994.2:c.2831G=	XP_011532296.1:p.Cys944=
NM_006514.4:c.3116G= MANE Select	NP_006505.4:p.Cys1039=