Canonical Allele Identifier: CA1358633378

Gene: SCN10A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38712346G= , CM000665.2:g.38712346G=	GRCh38
NC_000003.11:g.38753837G= , CM000665.1:g.38753837G=	GRCh37
NC_000003.10:g.38728841G=	NCBI36
NG_031891.2:g.86665C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000449082.3:c.3904C= MANE Select	ENSP00000390600.2:p.Leu1302=
ENST00000643924.1:c.3901C=	ENSP00000495595.1:p.Leu1301=
ENST00000655275.1:c.3928C=	ENSP00000499510.1:p.Leu1310=
ENST00000449082.2:c.3904C=	ENSP00000390600.2:p.Leu1302=
NM_001293306.2:c.3901C=	NP_001280235.2:p.Leu1301=
NM_001293307.2:c.3610C=	NP_001280236.2:p.Leu1204=
NM_006514.3:c.3904C=	NP_006505.3:p.Leu1302=
XM_005265371.2:c.3913C=	XP_005265428.1:p.Leu1305=
XM_011533993.1:c.3910C=	XP_011532295.1:p.Leu1304=
XM_011533994.1:c.3619C=	XP_011532296.1:p.Leu1207=
XM_005265371.3:c.3913C=	XP_005265428.1:p.Leu1305=
XM_011533993.2:c.3910C=	XP_011532295.1:p.Leu1304=
XM_011533994.2:c.3619C=	XP_011532296.1:p.Leu1207=
NM_006514.4:c.3904C= MANE Select	NP_006505.4:p.Leu1302=