Canonical Allele Identifier: CA352156803

Gene: SCN10A

Linked Data

• MyVariant Identifiers: chr3:g.38766779C>G (hg19) ; chr3:g.38725288C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38725288C>G , CM000665.2:g.38725288C>G	GRCh38
NC_000003.11:g.38766779C>G , CM000665.1:g.38766779C>G	GRCh37
NC_000003.10:g.38741783C>G	NCBI36
NG_031891.2:g.73723G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449082.3:c.3114G>C MANE Select	ENSP00000390600.2:p.Arg1038Ser
ENST00000643924.1:c.3111G>C	ENSP00000495595.1:p.Arg1037Ser
ENST00000655275.1:c.3138G>C	ENSP00000499510.1:p.Arg1046Ser
ENST00000449082.2:c.3114G>C	ENSP00000390600.2:p.Arg1038Ser
NM_001293306.2:c.3111G>C	NP_001280235.2:p.Arg1037Ser
NM_001293307.2:c.2820G>C	NP_001280236.2:p.Arg940Ser
NM_006514.3:c.3114G>C	NP_006505.3:p.Arg1038Ser
XM_005265371.2:c.3123G>C	XP_005265428.1:p.Arg1041Ser
XM_011533993.1:c.3120G>C	XP_011532295.1:p.Arg1040Ser
XM_011533994.1:c.2829G>C	XP_011532296.1:p.Arg943Ser
XM_005265371.3:c.3123G>C	XP_005265428.1:p.Arg1041Ser
XM_011533993.2:c.3120G>C	XP_011532295.1:p.Arg1040Ser
XM_011533994.2:c.2829G>C	XP_011532296.1:p.Arg943Ser
NM_006514.4:c.3114G>C MANE Select	NP_006505.4:p.Arg1038Ser