Canonical Allele Identifier: CA72986331

Gene: SCN10A

Linked Data

• ClinVar Variation Id: 579447
• ClinVar RCV Id: RCV000702732 ; RCV004026606
• dbSNP Id: rs535115766
• gnomAD v2: 3-38793732-G-A
• gnomAD v4: 3-38752241-G-A
• MyVariant Identifiers: chr3:g.38793732G>A (hg19) ; chr3:g.38752241G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38752241G>A , CM000665.2:g.38752241G>A	GRCh38
NC_000003.11:g.38793732G>A , CM000665.1:g.38793732G>A	GRCh37
NC_000003.10:g.38768736G>A	NCBI36
NG_031891.2:g.46770C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449082.3:c.1733C>T MANE Select	ENSP00000390600.2:p.Ala578Val
ENST00000643924.1:c.1733C>T	ENSP00000495595.1:p.Ala578Val
ENST00000655275.1:c.1760C>T	ENSP00000499510.1:p.Ala587Val
ENST00000449082.2:c.1733C>T	ENSP00000390600.2:p.Ala578Val
NM_001293306.2:c.1733C>T	NP_001280235.2:p.Ala578Val
NM_001293307.2:c.1462-2057C>T	NP_001280236.2:n.1462-2057C>T
NM_006514.3:c.1733C>T	NP_006505.3:p.Ala578Val
XM_005265371.2:c.1742C>T	XP_005265428.1:p.Ala581Val
XM_011533993.1:c.1742C>T	XP_011532295.1:p.Ala581Val
XM_011533994.1:c.1471-2057C>T	XP_011532296.1:n.1471-2057C>T
XM_005265371.3:c.1742C>T	XP_005265428.1:p.Ala581Val
XM_011533993.2:c.1742C>T	XP_011532295.1:p.Ala581Val
XM_011533994.2:c.1471-2057C>T	XP_011532296.1:n.1471-2057C>T
NM_006514.4:c.1733C>T MANE Select	NP_006505.4:p.Ala578Val