Canonical Allele Identifier: CA352167784

Gene: SCN10A

Linked Data

• MyVariant Identifiers: chr3:g.38793998A>T (hg19) ; chr3:g.38752507A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38752507A>T , CM000665.2:g.38752507A>T	GRCh38
NC_000003.11:g.38793998A>T , CM000665.1:g.38793998A>T	GRCh37
NC_000003.10:g.38769002A>T	NCBI36
NG_031891.2:g.46504T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449082.3:c.1467T>A MANE Select	ENSP00000390600.2:p.Phe489Leu
ENST00000643924.1:c.1467T>A	ENSP00000495595.1:p.Phe489Leu
ENST00000655275.1:c.1494T>A	ENSP00000499510.1:p.Phe498Leu
ENST00000449082.2:c.1467T>A	ENSP00000390600.2:p.Phe489Leu
NM_001293306.2:c.1467T>A	NP_001280235.2:p.Phe489Leu
NM_001293307.2:c.1462-2323T>A	NP_001280236.2:n.1462-2323T>A
NM_006514.3:c.1467T>A	NP_006505.3:p.Phe489Leu
XM_005265371.2:c.1476T>A	XP_005265428.1:p.Phe492Leu
XM_011533993.1:c.1476T>A	XP_011532295.1:p.Phe492Leu
XM_011533994.1:c.1471-2323T>A	XP_011532296.1:n.1471-2323T>A
XM_005265371.3:c.1476T>A	XP_005265428.1:p.Phe492Leu
XM_011533993.2:c.1476T>A	XP_011532295.1:p.Phe492Leu
XM_011533994.2:c.1471-2323T>A	XP_011532296.1:n.1471-2323T>A
NM_006514.4:c.1467T>A MANE Select	NP_006505.4:p.Phe489Leu