Canonical Allele Identifier: CA352167797

Gene: SCN10A

Linked Data

• MyVariant Identifiers: chr3:g.38794000A>T (hg19) ; chr3:g.38752509A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38752509A>T , CM000665.2:g.38752509A>T	GRCh38
NC_000003.11:g.38794000A>T , CM000665.1:g.38794000A>T	GRCh37
NC_000003.10:g.38769004A>T	NCBI36
NG_031891.2:g.46502T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449082.3:c.1465T>A MANE Select	ENSP00000390600.2:p.Phe489Ile
ENST00000643924.1:c.1465T>A	ENSP00000495595.1:p.Phe489Ile
ENST00000655275.1:c.1492T>A	ENSP00000499510.1:p.Phe498Ile
ENST00000449082.2:c.1465T>A	ENSP00000390600.2:p.Phe489Ile
NM_001293306.2:c.1465T>A	NP_001280235.2:p.Phe489Ile
NM_001293307.2:c.1462-2325T>A	NP_001280236.2:n.1462-2325T>A
NM_006514.3:c.1465T>A	NP_006505.3:p.Phe489Ile
XM_005265371.2:c.1474T>A	XP_005265428.1:p.Phe492Ile
XM_011533993.1:c.1474T>A	XP_011532295.1:p.Phe492Ile
XM_011533994.1:c.1471-2325T>A	XP_011532296.1:n.1471-2325T>A
XM_005265371.3:c.1474T>A	XP_005265428.1:p.Phe492Ile
XM_011533993.2:c.1474T>A	XP_011532295.1:p.Phe492Ile
XM_011533994.2:c.1471-2325T>A	XP_011532296.1:n.1471-2325T>A
NM_006514.4:c.1465T>A MANE Select	NP_006505.4:p.Phe489Ile