Canonical Allele Identifier: CA1358640608

Gene: SCN10A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38725308G= , CM000665.2:g.38725308G=	GRCh38
NC_000003.11:g.38766799G= , CM000665.1:g.38766799G=	GRCh37
NC_000003.10:g.38741803G=	NCBI36
NG_031891.2:g.73703C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449082.3:c.3094C= MANE Select	ENSP00000390600.2:p.Gln1032=
ENST00000643924.1:c.3091C=	ENSP00000495595.1:p.Gln1031=
ENST00000655275.1:c.3118C=	ENSP00000499510.1:p.Gln1040=
ENST00000449082.2:c.3094C=	ENSP00000390600.2:p.Gln1032=
NM_001293306.2:c.3091C=	NP_001280235.2:p.Gln1031=
NM_001293307.2:c.2800C=	NP_001280236.2:p.Gln934=
NM_006514.3:c.3094C=	NP_006505.3:p.Gln1032=
XM_005265371.2:c.3103C=	XP_005265428.1:p.Gln1035=
XM_011533993.1:c.3100C=	XP_011532295.1:p.Gln1034=
XM_011533994.1:c.2809C=	XP_011532296.1:p.Gln937=
XM_005265371.3:c.3103C=	XP_005265428.1:p.Gln1035=
XM_011533993.2:c.3100C=	XP_011532295.1:p.Gln1034=
XM_011533994.2:c.2809C=	XP_011532296.1:p.Gln937=
NM_006514.4:c.3094C= MANE Select	NP_006505.4:p.Gln1032=