Canonical Allele Identifier: CA433138230

Gene: SCN10A

Linked Data

• gnomAD v4: 3-38723518-C-A
• MyVariant Identifiers: chr3:g.38765009C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38723518C>A , CM000665.2:g.38723518C>A	GRCh38
NC_000003.11:g.38765009C>A , CM000665.1:g.38765009C>A	GRCh37
NC_000003.10:g.38740013C>A	NCBI36
NG_031891.2:g.75493G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449082.3:c.3264G>T MANE Select	ENSP00000390600.2:p.Thr1088=
ENST00000643924.1:c.3261G>T	ENSP00000495595.1:p.Thr1087=
ENST00000655275.1:c.3288G>T	ENSP00000499510.1:p.Thr1096=
ENST00000449082.2:c.3264G>T	ENSP00000390600.2:p.Thr1088=
NM_001293306.2:c.3261G>T	NP_001280235.2:p.Thr1087=
NM_001293307.2:c.2970G>T	NP_001280236.2:p.Thr990=
NM_006514.3:c.3264G>T	NP_006505.3:p.Thr1088=
XM_005265371.2:c.3273G>T	XP_005265428.1:p.Thr1091=
XM_011533993.1:c.3270G>T	XP_011532295.1:p.Thr1090=
XM_011533994.1:c.2979G>T	XP_011532296.1:p.Thr993=
XM_005265371.3:c.3273G>T	XP_005265428.1:p.Thr1091=
XM_011533993.2:c.3270G>T	XP_011532295.1:p.Thr1090=
XM_011533994.2:c.2979G>T	XP_011532296.1:p.Thr993=
NM_006514.4:c.3264G>T MANE Select	NP_006505.4:p.Thr1088=