Canonical Allele Identifier: CA352167650

Gene: SCN10A

Linked Data

• MyVariant Identifiers: chr3:g.38793952A>C (hg19) ; chr3:g.38752461A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38752461A>C , CM000665.2:g.38752461A>C	GRCh38
NC_000003.11:g.38793952A>C , CM000665.1:g.38793952A>C	GRCh37
NC_000003.10:g.38768956A>C	NCBI36
NG_031891.2:g.46550T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449082.3:c.1513T>G MANE Select	ENSP00000390600.2:p.Phe505Val
ENST00000643924.1:c.1513T>G	ENSP00000495595.1:p.Phe505Val
ENST00000655275.1:c.1540T>G	ENSP00000499510.1:p.Phe514Val
ENST00000449082.2:c.1513T>G	ENSP00000390600.2:p.Phe505Val
NM_001293306.2:c.1513T>G	NP_001280235.2:p.Phe505Val
NM_001293307.2:c.1462-2277T>G	NP_001280236.2:n.1462-2277T>G
NM_006514.3:c.1513T>G	NP_006505.3:p.Phe505Val
XM_005265371.2:c.1522T>G	XP_005265428.1:p.Phe508Val
XM_011533993.1:c.1522T>G	XP_011532295.1:p.Phe508Val
XM_011533994.1:c.1471-2277T>G	XP_011532296.1:n.1471-2277T>G
XM_005265371.3:c.1522T>G	XP_005265428.1:p.Phe508Val
XM_011533993.2:c.1522T>G	XP_011532295.1:p.Phe508Val
XM_011533994.2:c.1471-2277T>G	XP_011532296.1:n.1471-2277T>G
NM_006514.4:c.1513T>G MANE Select	NP_006505.4:p.Phe505Val