Canonical Allele Identifier: CA352156855

Gene: SCN10A

Linked Data

• MyVariant Identifiers: chr3:g.38766802C>G (hg19) ; chr3:g.38725311C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38725311C>G , CM000665.2:g.38725311C>G	GRCh38
NC_000003.11:g.38766802C>G , CM000665.1:g.38766802C>G	GRCh37
NC_000003.10:g.38741806C>G	NCBI36
NG_031891.2:g.73700G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449082.3:c.3091G>C MANE Select	ENSP00000390600.2:p.Glu1031Gln
ENST00000643924.1:c.3088G>C	ENSP00000495595.1:p.Glu1030Gln
ENST00000655275.1:c.3115G>C	ENSP00000499510.1:p.Glu1039Gln
ENST00000449082.2:c.3091G>C	ENSP00000390600.2:p.Glu1031Gln
NM_001293306.2:c.3088G>C	NP_001280235.2:p.Glu1030Gln
NM_001293307.2:c.2797G>C	NP_001280236.2:p.Glu933Gln
NM_006514.3:c.3091G>C	NP_006505.3:p.Glu1031Gln
XM_005265371.2:c.3100G>C	XP_005265428.1:p.Glu1034Gln
XM_011533993.1:c.3097G>C	XP_011532295.1:p.Glu1033Gln
XM_011533994.1:c.2806G>C	XP_011532296.1:p.Glu936Gln
XM_005265371.3:c.3100G>C	XP_005265428.1:p.Glu1034Gln
XM_011533993.2:c.3097G>C	XP_011532295.1:p.Glu1033Gln
XM_011533994.2:c.2806G>C	XP_011532296.1:p.Glu936Gln
NM_006514.4:c.3091G>C MANE Select	NP_006505.4:p.Glu1031Gln