Canonical Allele Identifier: CA1358639729

Gene: SCN10A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38723467T= , CM000665.2:g.38723467T=	GRCh38
NC_000003.11:g.38764958T= , CM000665.1:g.38764958T=	GRCh37
NC_000003.10:g.38739962T=	NCBI36
NG_031891.2:g.75544A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449082.3:c.3315A= MANE Select	ENSP00000390600.2:p.Ala1105=
ENST00000643924.1:c.3312A=	ENSP00000495595.1:p.Ala1104=
ENST00000655275.1:c.3339A=	ENSP00000499510.1:p.Ala1113=
ENST00000449082.2:c.3315A=	ENSP00000390600.2:p.Ala1105=
NM_001293306.2:c.3312A=	NP_001280235.2:p.Ala1104=
NM_001293307.2:c.3021A=	NP_001280236.2:p.Ala1007=
NM_006514.3:c.3315A=	NP_006505.3:p.Ala1105=
XM_005265371.2:c.3324A=	XP_005265428.1:p.Ala1108=
XM_011533993.1:c.3321A=	XP_011532295.1:p.Ala1107=
XM_011533994.1:c.3030A=	XP_011532296.1:p.Ala1010=
XM_005265371.3:c.3324A=	XP_005265428.1:p.Ala1108=
XM_011533993.2:c.3321A=	XP_011532295.1:p.Ala1107=
XM_011533994.2:c.3030A=	XP_011532296.1:p.Ala1010=
NM_006514.4:c.3315A= MANE Select	NP_006505.4:p.Ala1105=