Canonical Allele Identifier: CA72958398

Gene: SCN10A

Linked Data

• dbSNP Id: rs776762727
• gnomAD v4: 3-38723370-T-C
• MyVariant Identifiers: chr3:g.38764861T>C (hg19) ; chr3:g.38723370T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38723370T>C , CM000665.2:g.38723370T>C	GRCh38
NC_000003.11:g.38764861T>C , CM000665.1:g.38764861T>C	GRCh37
NC_000003.10:g.38739865T>C	NCBI36
NG_031891.2:g.75641A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449082.3:c.3352+60A>G MANE Select	ENSP00000390600.2:n.3352+60A>G
ENST00000643924.1:c.3349+60A>G	ENSP00000495595.1:n.3349+60A>G
ENST00000655275.1:c.3376+60A>G	ENSP00000499510.1:n.3376+60A>G
ENST00000449082.2:c.3352+60A>G	ENSP00000390600.2:n.3352+60A>G
NM_001293306.2:c.3349+60A>G	NP_001280235.2:n.3349+60A>G
NM_001293307.2:c.3058+60A>G	NP_001280236.2:n.3058+60A>G
NM_006514.3:c.3352+60A>G	NP_006505.3:n.3352+60A>G
XM_005265371.2:c.3361+60A>G	XP_005265428.1:n.3361+60A>G
XM_011533993.1:c.3358+60A>G	XP_011532295.1:n.3358+60A>G
XM_011533994.1:c.3067+60A>G	XP_011532296.1:n.3067+60A>G
XM_005265371.3:c.3361+60A>G	XP_005265428.1:n.3361+60A>G
XM_011533993.2:c.3358+60A>G	XP_011532295.1:n.3358+60A>G
XM_011533994.2:c.3067+60A>G	XP_011532296.1:n.3067+60A>G
NM_006514.4:c.3352+60A>G MANE Select	NP_006505.4:n.3352+60A>G