Canonical Allele Identifier: CA352156830

Gene: SCN10A

Linked Data

• gnomAD v4: 3-38725300-C-A
• MyVariant Identifiers: chr3:g.38766791C>A (hg19) ; chr3:g.38725300C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38725300C>A , CM000665.2:g.38725300C>A	GRCh38
NC_000003.11:g.38766791C>A , CM000665.1:g.38766791C>A	GRCh37
NC_000003.10:g.38741795C>A	NCBI36
NG_031891.2:g.73711G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449082.3:c.3102G>T MANE Select	ENSP00000390600.2:p.Gln1034His
ENST00000643924.1:c.3099G>T	ENSP00000495595.1:p.Gln1033His
ENST00000655275.1:c.3126G>T	ENSP00000499510.1:p.Gln1042His
ENST00000449082.2:c.3102G>T	ENSP00000390600.2:p.Gln1034His
NM_001293306.2:c.3099G>T	NP_001280235.2:p.Gln1033His
NM_001293307.2:c.2808G>T	NP_001280236.2:p.Gln936His
NM_006514.3:c.3102G>T	NP_006505.3:p.Gln1034His
XM_005265371.2:c.3111G>T	XP_005265428.1:p.Gln1037His
XM_011533993.1:c.3108G>T	XP_011532295.1:p.Gln1036His
XM_011533994.1:c.2817G>T	XP_011532296.1:p.Gln939His
XM_005265371.3:c.3111G>T	XP_005265428.1:p.Gln1037His
XM_011533993.2:c.3108G>T	XP_011532295.1:p.Gln1036His
XM_011533994.2:c.2817G>T	XP_011532296.1:p.Gln939His
NM_006514.4:c.3102G>T MANE Select	NP_006505.4:p.Gln1034His