Canonical Allele Identifier: CA1358633369

Gene: SCN10A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38712340C= , CM000665.2:g.38712340C=	GRCh38
NC_000003.11:g.38753831C= , CM000665.1:g.38753831C=	GRCh37
NC_000003.10:g.38728835C=	NCBI36
NG_031891.2:g.86671G=

Transcript Alleles

HGVS	Amino-acid Change
NM_006514.4:c.3910G= MANE Select	NP_006505.4:p.Ala1304=
ENST00000449082.3:c.3910G= MANE Select	ENSP00000390600.2:p.Ala1304=
NM_001293306.2:c.3907G=	NP_001280235.2:p.Ala1303=
NM_001293307.2:c.3616G=	NP_001280236.2:p.Ala1206=
NM_006514.3:c.3910G=	NP_006505.3:p.Ala1304=
ENST00000449082.2:c.3910G=	ENSP00000390600.2:p.Ala1304=
ENST00000643924.1:c.3907G=	ENSP00000495595.1:p.Ala1303=
ENST00000655275.1:c.3934G=	ENSP00000499510.1:p.Ala1312=
XM_005265371.2:c.3919G=	XP_005265428.1:p.Ala1307=
XM_005265371.3:c.3919G=	XP_005265428.1:p.Ala1307=
XM_011533993.1:c.3916G=	XP_011532295.1:p.Ala1306=
XM_011533993.2:c.3916G=	XP_011532295.1:p.Ala1306=
XM_011533994.1:c.3625G=	XP_011532296.1:p.Ala1209=
XM_011533994.2:c.3625G=	XP_011532296.1:p.Ala1209=