Canonical Allele Identifier: CA352155968

Gene: SCN10A

Linked Data

• gnomAD v4: 3-38723430-C-T
• MyVariant Identifiers: chr3:g.38764921C>T (hg19) ; chr3:g.38723430C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38723430C>T , CM000665.2:g.38723430C>T	GRCh38
NC_000003.11:g.38764921C>T , CM000665.1:g.38764921C>T	GRCh37
NC_000003.10:g.38739925C>T	NCBI36
NG_031891.2:g.75581G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449082.3:c.3352G>A MANE Select	ENSP00000390600.2:p.Gly1118Arg
ENST00000643924.1:c.3349G>A	ENSP00000495595.1:p.Gly1117Arg
ENST00000655275.1:c.3376G>A	ENSP00000499510.1:p.Gly1126Arg
ENST00000449082.2:c.3352G>A	ENSP00000390600.2:p.Gly1118Arg
NM_001293306.2:c.3349G>A	NP_001280235.2:p.Gly1117Arg
NM_001293307.2:c.3058G>A	NP_001280236.2:p.Gly1020Arg
NM_006514.3:c.3352G>A	NP_006505.3:p.Gly1118Arg
XM_005265371.2:c.3361G>A	XP_005265428.1:p.Gly1121Arg
XM_011533993.1:c.3358G>A	XP_011532295.1:p.Gly1120Arg
XM_011533994.1:c.3067G>A	XP_011532296.1:p.Gly1023Arg
XM_005265371.3:c.3361G>A	XP_005265428.1:p.Gly1121Arg
XM_011533993.2:c.3358G>A	XP_011532295.1:p.Gly1120Arg
XM_011533994.2:c.3067G>A	XP_011532296.1:p.Gly1023Arg
NM_006514.4:c.3352G>A MANE Select	NP_006505.4:p.Gly1118Arg