Canonical Allele Identifier: CA1358653327

Gene: SCN10A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38752477A= , CM000665.2:g.38752477A=	GRCh38
NC_000003.11:g.38793968A= , CM000665.1:g.38793968A=	GRCh37
NC_000003.10:g.38768972A=	NCBI36
NG_031891.2:g.46534T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449082.3:c.1497T= MANE Select	ENSP00000390600.2:p.Ala499=
ENST00000643924.1:c.1497T=	ENSP00000495595.1:p.Ala499=
ENST00000655275.1:c.1524T=	ENSP00000499510.1:p.Ala508=
ENST00000449082.2:c.1497T=	ENSP00000390600.2:p.Ala499=
NM_001293306.2:c.1497T=	NP_001280235.2:p.Ala499=
NM_001293307.2:c.1462-2293T=	NP_001280236.2:n.1462-2293T=
NM_006514.3:c.1497T=	NP_006505.3:p.Ala499=
XM_005265371.2:c.1506T=	XP_005265428.1:p.Ala502=
XM_011533993.1:c.1506T=	XP_011532295.1:p.Ala502=
XM_011533994.1:c.1471-2293T=	XP_011532296.1:n.1471-2293T=
XM_005265371.3:c.1506T=	XP_005265428.1:p.Ala502=
XM_011533993.2:c.1506T=	XP_011532295.1:p.Ala502=
XM_011533994.2:c.1471-2293T=	XP_011532296.1:n.1471-2293T=
NM_006514.4:c.1497T= MANE Select	NP_006505.4:p.Ala499=