Canonical Allele Identifier: CA1358640577

Gene: SCN10A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38725245A= , CM000665.2:g.38725245A=	GRCh38
NC_000003.11:g.38766736A= , CM000665.1:g.38766736A=	GRCh37
NC_000003.10:g.38741740A=	NCBI36
NG_031891.2:g.73766T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449082.3:c.3157T= MANE Select	ENSP00000390600.2:p.Ser1053=
ENST00000643924.1:c.3154T=	ENSP00000495595.1:p.Ser1052=
ENST00000655275.1:c.3181T=	ENSP00000499510.1:p.Ser1061=
ENST00000449082.2:c.3157T=	ENSP00000390600.2:p.Ser1053=
NM_001293306.2:c.3154T=	NP_001280235.2:p.Ser1052=
NM_001293307.2:c.2863T=	NP_001280236.2:p.Ser955=
NM_006514.3:c.3157T=	NP_006505.3:p.Ser1053=
XM_005265371.2:c.3166T=	XP_005265428.1:p.Ser1056=
XM_011533993.1:c.3163T=	XP_011532295.1:p.Ser1055=
XM_011533994.1:c.2872T=	XP_011532296.1:p.Ser958=
XM_005265371.3:c.3166T=	XP_005265428.1:p.Ser1056=
XM_011533993.2:c.3163T=	XP_011532295.1:p.Ser1055=
XM_011533994.2:c.2872T=	XP_011532296.1:p.Ser958=
NM_006514.4:c.3157T= MANE Select	NP_006505.4:p.Ser1053=