Canonical Allele Identifier: CA1358640818

Gene: SCN10A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38725753A= , CM000665.2:g.38725753A=	GRCh38
NC_000003.11:g.38767244A= , CM000665.1:g.38767244A=	GRCh37
NC_000003.10:g.38742248A=	NCBI36
NG_031891.2:g.73258T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449082.3:c.3088-439T= MANE Select	ENSP00000390600.2:n.3088-439T=
ENST00000643924.1:c.3088-442T=	ENSP00000495595.1:n.3088-442T=
ENST00000655275.1:c.3115-442T=	ENSP00000499510.1:n.3115-442T=
ENST00000449082.2:c.3088-439T=	ENSP00000390600.2:n.3088-439T=
NM_001293306.2:c.3088-442T=	NP_001280235.2:n.3088-442T=
NM_001293307.2:c.2794-439T=	NP_001280236.2:n.2794-439T=
NM_006514.3:c.3088-439T=	NP_006505.3:n.3088-439T=
XM_005265371.2:c.3097-439T=	XP_005265428.1:n.3097-439T=
XM_011533993.1:c.3097-442T=	XP_011532295.1:n.3097-442T=
XM_011533994.1:c.2803-439T=	XP_011532296.1:n.2803-439T=
XM_005265371.3:c.3097-439T=	XP_005265428.1:n.3097-439T=
XM_011533993.2:c.3097-442T=	XP_011532295.1:n.3097-442T=
XM_011533994.2:c.2803-439T=	XP_011532296.1:n.2803-439T=
NM_006514.4:c.3088-439T= MANE Select	NP_006505.4:n.3088-439T=