Canonical Allele Identifier: CA433138495

Gene: SCN10A

Linked Data

• MyVariant Identifiers: chr3:g.38766713G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38725222G>C , CM000665.2:g.38725222G>C	GRCh38
NC_000003.11:g.38766713G>C , CM000665.1:g.38766713G>C	GRCh37
NC_000003.10:g.38741717G>C	NCBI36
NG_031891.2:g.73789C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449082.3:c.3180C>G MANE Select	ENSP00000390600.2:p.Ser1060=
ENST00000643924.1:c.3177C>G	ENSP00000495595.1:p.Ser1059=
ENST00000655275.1:c.3204C>G	ENSP00000499510.1:p.Ser1068=
ENST00000449082.2:c.3180C>G	ENSP00000390600.2:p.Ser1060=
NM_001293306.2:c.3177C>G	NP_001280235.2:p.Ser1059=
NM_001293307.2:c.2886C>G	NP_001280236.2:p.Ser962=
NM_006514.3:c.3180C>G	NP_006505.3:p.Ser1060=
XM_005265371.2:c.3189C>G	XP_005265428.1:p.Ser1063=
XM_011533993.1:c.3186C>G	XP_011532295.1:p.Ser1062=
XM_011533994.1:c.2895C>G	XP_011532296.1:p.Ser965=
XM_005265371.3:c.3189C>G	XP_005265428.1:p.Ser1063=
XM_011533993.2:c.3186C>G	XP_011532295.1:p.Ser1062=
XM_011533994.2:c.2895C>G	XP_011532296.1:p.Ser965=
NM_006514.4:c.3180C>G MANE Select	NP_006505.4:p.Ser1060=