Canonical Allele Identifier: CA433138489

Gene: SCN10A

Linked Data

• MyVariant Identifiers: chr3:g.38766707A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38725216A>T , CM000665.2:g.38725216A>T	GRCh38
NC_000003.11:g.38766707A>T , CM000665.1:g.38766707A>T	GRCh37
NC_000003.10:g.38741711A>T	NCBI36
NG_031891.2:g.73795T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449082.3:c.3186T>A MANE Select	ENSP00000390600.2:p.Gly1062=
ENST00000643924.1:c.3183T>A	ENSP00000495595.1:p.Gly1061=
ENST00000655275.1:c.3210T>A	ENSP00000499510.1:p.Gly1070=
ENST00000449082.2:c.3186T>A	ENSP00000390600.2:p.Gly1062=
NM_001293306.2:c.3183T>A	NP_001280235.2:p.Gly1061=
NM_001293307.2:c.2892T>A	NP_001280236.2:p.Gly964=
NM_006514.3:c.3186T>A	NP_006505.3:p.Gly1062=
XM_005265371.2:c.3195T>A	XP_005265428.1:p.Gly1065=
XM_011533993.1:c.3192T>A	XP_011532295.1:p.Gly1064=
XM_011533994.1:c.2901T>A	XP_011532296.1:p.Gly967=
XM_005265371.3:c.3195T>A	XP_005265428.1:p.Gly1065=
XM_011533993.2:c.3192T>A	XP_011532295.1:p.Gly1064=
XM_011533994.2:c.2901T>A	XP_011532296.1:p.Gly967=
NM_006514.4:c.3186T>A MANE Select	NP_006505.4:p.Gly1062=