Canonical Allele Identifier: CA433138128

Gene: SCN10A

Linked Data

• MyVariant Identifiers: chr3:g.38764925T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38723434T>G , CM000665.2:g.38723434T>G	GRCh38
NC_000003.11:g.38764925T>G , CM000665.1:g.38764925T>G	GRCh37
NC_000003.10:g.38739929T>G	NCBI36
NG_031891.2:g.75577A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000449082.3:c.3348A>C MANE Select	ENSP00000390600.2:p.Thr1116=
ENST00000643924.1:c.3345A>C	ENSP00000495595.1:p.Thr1115=
ENST00000655275.1:c.3372A>C	ENSP00000499510.1:p.Thr1124=
ENST00000449082.2:c.3348A>C	ENSP00000390600.2:p.Thr1116=
NM_001293306.2:c.3345A>C	NP_001280235.2:p.Thr1115=
NM_001293307.2:c.3054A>C	NP_001280236.2:p.Thr1018=
NM_006514.3:c.3348A>C	NP_006505.3:p.Thr1116=
XM_005265371.2:c.3357A>C	XP_005265428.1:p.Thr1119=
XM_011533993.1:c.3354A>C	XP_011532295.1:p.Thr1118=
XM_011533994.1:c.3063A>C	XP_011532296.1:p.Thr1021=
XM_005265371.3:c.3357A>C	XP_005265428.1:p.Thr1119=
XM_011533993.2:c.3354A>C	XP_011532295.1:p.Thr1118=
XM_011533994.2:c.3063A>C	XP_011532296.1:p.Thr1021=
NM_006514.4:c.3348A>C MANE Select	NP_006505.4:p.Thr1116=