Canonical Allele Identifier: CA433138502

Gene: SCN10A

Linked Data

• MyVariant Identifiers: chr3:g.38766722C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38725231C>G , CM000665.2:g.38725231C>G	GRCh38
NC_000003.11:g.38766722C>G , CM000665.1:g.38766722C>G	GRCh37
NC_000003.10:g.38741726C>G	NCBI36
NG_031891.2:g.73780G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449082.3:c.3171G>C MANE Select	ENSP00000390600.2:p.Leu1057=
ENST00000643924.1:c.3168G>C	ENSP00000495595.1:p.Leu1056=
ENST00000655275.1:c.3195G>C	ENSP00000499510.1:p.Leu1065=
ENST00000449082.2:c.3171G>C	ENSP00000390600.2:p.Leu1057=
NM_001293306.2:c.3168G>C	NP_001280235.2:p.Leu1056=
NM_001293307.2:c.2877G>C	NP_001280236.2:p.Leu959=
NM_006514.3:c.3171G>C	NP_006505.3:p.Leu1057=
XM_005265371.2:c.3180G>C	XP_005265428.1:p.Leu1060=
XM_011533993.1:c.3177G>C	XP_011532295.1:p.Leu1059=
XM_011533994.1:c.2886G>C	XP_011532296.1:p.Leu962=
XM_005265371.3:c.3180G>C	XP_005265428.1:p.Leu1060=
XM_011533993.2:c.3177G>C	XP_011532295.1:p.Leu1059=
XM_011533994.2:c.2886G>C	XP_011532296.1:p.Leu962=
NM_006514.4:c.3171G>C MANE Select	NP_006505.4:p.Leu1057=