Canonical Allele Identifier: CA352155091

Gene: SCN10A

Linked Data

• dbSNP Id: rs2063118614
• MyVariant Identifiers: chr3:g.38739783T>C (hg19) ; chr3:g.38698292T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38698292T>C , CM000665.2:g.38698292T>C	GRCh38
NC_000003.11:g.38739783T>C , CM000665.1:g.38739783T>C	GRCh37
NC_000003.10:g.38714787T>C	NCBI36
NG_031891.2:g.100719A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449082.3:c.4928A>G MANE Select	ENSP00000390600.2:p.Asn1643Ser
ENST00000643924.1:c.4925A>G	ENSP00000495595.1:p.Asn1642Ser
ENST00000655275.1:c.4952A>G	ENSP00000499510.1:p.Asn1651Ser
ENST00000449082.2:c.4928A>G	ENSP00000390600.2:p.Asn1643Ser
NM_001293306.2:c.4925A>G	NP_001280235.2:p.Asn1642Ser
NM_001293307.2:c.4634A>G	NP_001280236.2:p.Asn1545Ser
NM_006514.3:c.4928A>G	NP_006505.3:p.Asn1643Ser
XM_005265371.2:c.4937A>G	XP_005265428.1:p.Asn1646Ser
XM_011533993.1:c.4934A>G	XP_011532295.1:p.Asn1645Ser
XM_011533994.1:c.4643A>G	XP_011532296.1:p.Asn1548Ser
XM_005265371.3:c.4937A>G	XP_005265428.1:p.Asn1646Ser
XM_011533993.2:c.4934A>G	XP_011532295.1:p.Asn1645Ser
XM_011533994.2:c.4643A>G	XP_011532296.1:p.Asn1548Ser
NM_006514.4:c.4928A>G MANE Select	NP_006505.4:p.Asn1643Ser