Canonical Allele Identifier: CA352156203

Gene: SCN10A

Linked Data

• dbSNP Id: rs1331382578
• MyVariant Identifiers: chr3:g.38764966C>T (hg19) ; chr3:g.38723475C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38723475C>T , CM000665.2:g.38723475C>T	GRCh38
NC_000003.11:g.38764966C>T , CM000665.1:g.38764966C>T	GRCh37
NC_000003.10:g.38739970C>T	NCBI36
NG_031891.2:g.75536G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449082.3:c.3307G>A MANE Select	ENSP00000390600.2:p.Glu1103Lys
ENST00000643924.1:c.3304G>A	ENSP00000495595.1:p.Glu1102Lys
ENST00000655275.1:c.3331G>A	ENSP00000499510.1:p.Glu1111Lys
ENST00000449082.2:c.3307G>A	ENSP00000390600.2:p.Glu1103Lys
NM_001293306.2:c.3304G>A	NP_001280235.2:p.Glu1102Lys
NM_001293307.2:c.3013G>A	NP_001280236.2:p.Glu1005Lys
NM_006514.3:c.3307G>A	NP_006505.3:p.Glu1103Lys
XM_005265371.2:c.3316G>A	XP_005265428.1:p.Glu1106Lys
XM_011533993.1:c.3313G>A	XP_011532295.1:p.Glu1105Lys
XM_011533994.1:c.3022G>A	XP_011532296.1:p.Glu1008Lys
XM_005265371.3:c.3316G>A	XP_005265428.1:p.Glu1106Lys
XM_011533993.2:c.3313G>A	XP_011532295.1:p.Glu1105Lys
XM_011533994.2:c.3022G>A	XP_011532296.1:p.Glu1008Lys
NM_006514.4:c.3307G>A MANE Select	NP_006505.4:p.Glu1103Lys