Canonical Allele Identifier: CA352156765

Gene: SCN10A

Linked Data

• MyVariant Identifiers: chr3:g.38766762G>C (hg19) ; chr3:g.38725271G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38725271G>C , CM000665.2:g.38725271G>C	GRCh38
NC_000003.11:g.38766762G>C , CM000665.1:g.38766762G>C	GRCh37
NC_000003.10:g.38741766G>C	NCBI36
NG_031891.2:g.73740C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449082.3:c.3131C>G MANE Select	ENSP00000390600.2:p.Thr1044Arg
ENST00000643924.1:c.3128C>G	ENSP00000495595.1:p.Thr1043Arg
ENST00000655275.1:c.3155C>G	ENSP00000499510.1:p.Thr1052Arg
ENST00000449082.2:c.3131C>G	ENSP00000390600.2:p.Thr1044Arg
NM_001293306.2:c.3128C>G	NP_001280235.2:p.Thr1043Arg
NM_001293307.2:c.2837C>G	NP_001280236.2:p.Thr946Arg
NM_006514.3:c.3131C>G	NP_006505.3:p.Thr1044Arg
XM_005265371.2:c.3140C>G	XP_005265428.1:p.Thr1047Arg
XM_011533993.1:c.3137C>G	XP_011532295.1:p.Thr1046Arg
XM_011533994.1:c.2846C>G	XP_011532296.1:p.Thr949Arg
XM_005265371.3:c.3140C>G	XP_005265428.1:p.Thr1047Arg
XM_011533993.2:c.3137C>G	XP_011532295.1:p.Thr1046Arg
XM_011533994.2:c.2846C>G	XP_011532296.1:p.Thr949Arg
NM_006514.4:c.3131C>G MANE Select	NP_006505.4:p.Thr1044Arg