Canonical Allele Identifier: CA352156747

Gene: SCN10A

Linked Data

• MyVariant Identifiers: chr3:g.38766752G>T (hg19) ; chr3:g.38725261G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38725261G>T , CM000665.2:g.38725261G>T	GRCh38
NC_000003.11:g.38766752G>T , CM000665.1:g.38766752G>T	GRCh37
NC_000003.10:g.38741756G>T	NCBI36
NG_031891.2:g.73750C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449082.3:c.3141C>A MANE Select	ENSP00000390600.2:p.Ser1047Arg
ENST00000643924.1:c.3138C>A	ENSP00000495595.1:p.Ser1046Arg
ENST00000655275.1:c.3165C>A	ENSP00000499510.1:p.Ser1055Arg
ENST00000449082.2:c.3141C>A	ENSP00000390600.2:p.Ser1047Arg
NM_001293306.2:c.3138C>A	NP_001280235.2:p.Ser1046Arg
NM_001293307.2:c.2847C>A	NP_001280236.2:p.Ser949Arg
NM_006514.3:c.3141C>A	NP_006505.3:p.Ser1047Arg
XM_005265371.2:c.3150C>A	XP_005265428.1:p.Ser1050Arg
XM_011533993.1:c.3147C>A	XP_011532295.1:p.Ser1049Arg
XM_011533994.1:c.2856C>A	XP_011532296.1:p.Ser952Arg
XM_005265371.3:c.3150C>A	XP_005265428.1:p.Ser1050Arg
XM_011533993.2:c.3147C>A	XP_011532295.1:p.Ser1049Arg
XM_011533994.2:c.2856C>A	XP_011532296.1:p.Ser952Arg
NM_006514.4:c.3141C>A MANE Select	NP_006505.4:p.Ser1047Arg