Canonical Allele Identifier: CA352151209

Gene: SCN10A

Linked Data

• MyVariant Identifiers: chr3:g.38753839T>A (hg19) ; chr3:g.38712348T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38712348T>A , CM000665.2:g.38712348T>A	GRCh38
NC_000003.11:g.38753839T>A , CM000665.1:g.38753839T>A	GRCh37
NC_000003.10:g.38728843T>A	NCBI36
NG_031891.2:g.86663A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000449082.3:c.3902A>T MANE Select	ENSP00000390600.2:p.Asn1301Ile
ENST00000643924.1:c.3899A>T	ENSP00000495595.1:p.Asn1300Ile
ENST00000655275.1:c.3926A>T	ENSP00000499510.1:p.Asn1309Ile
ENST00000449082.2:c.3902A>T	ENSP00000390600.2:p.Asn1301Ile
NM_001293306.2:c.3899A>T	NP_001280235.2:p.Asn1300Ile
NM_001293307.2:c.3608A>T	NP_001280236.2:p.Asn1203Ile
NM_006514.3:c.3902A>T	NP_006505.3:p.Asn1301Ile
XM_005265371.2:c.3911A>T	XP_005265428.1:p.Asn1304Ile
XM_011533993.1:c.3908A>T	XP_011532295.1:p.Asn1303Ile
XM_011533994.1:c.3617A>T	XP_011532296.1:p.Asn1206Ile
XM_005265371.3:c.3911A>T	XP_005265428.1:p.Asn1304Ile
XM_011533993.2:c.3908A>T	XP_011532295.1:p.Asn1303Ile
XM_011533994.2:c.3617A>T	XP_011532296.1:p.Asn1206Ile
NM_006514.4:c.3902A>T MANE Select	NP_006505.4:p.Asn1301Ile