Canonical Allele Identifier: CA433333995

Gene: SCN10A

Linked Data

• MyVariant Identifiers: chr3:g.38753841C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38712350C>T , CM000665.2:g.38712350C>T	GRCh38
NC_000003.11:g.38753841C>T , CM000665.1:g.38753841C>T	GRCh37
NC_000003.10:g.38728845C>T	NCBI36
NG_031891.2:g.86661G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000449082.3:c.3900G>A MANE Select	ENSP00000390600.2:p.Val1300=
ENST00000643924.1:c.3897G>A	ENSP00000495595.1:p.Val1299=
ENST00000655275.1:c.3924G>A	ENSP00000499510.1:p.Val1308=
ENST00000449082.2:c.3900G>A	ENSP00000390600.2:p.Val1300=
NM_001293306.2:c.3897G>A	NP_001280235.2:p.Val1299=
NM_001293307.2:c.3606G>A	NP_001280236.2:p.Val1202=
NM_006514.3:c.3900G>A	NP_006505.3:p.Val1300=
XM_005265371.2:c.3909G>A	XP_005265428.1:p.Val1303=
XM_011533993.1:c.3906G>A	XP_011532295.1:p.Val1302=
XM_011533994.1:c.3615G>A	XP_011532296.1:p.Val1205=
XM_005265371.3:c.3909G>A	XP_005265428.1:p.Val1303=
XM_011533993.2:c.3906G>A	XP_011532295.1:p.Val1302=
XM_011533994.2:c.3615G>A	XP_011532296.1:p.Val1205=
NM_006514.4:c.3900G>A MANE Select	NP_006505.4:p.Val1300=