Canonical Allele Identifier: CA2665100305

Gene: SCN10A

Linked Data

• gnomAD v4: 3-38725403-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38725403_38725404insA , CM000665.2:g.38725403_38725404insA	GRCh38
NC_000003.11:g.38766894_38766895insA , CM000665.1:g.38766894_38766895insA	GRCh37
NC_000003.10:g.38741898_38741899insA	NCBI36
NG_031891.2:g.73607_73608insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449082.3:c.3088-90_3088-89insT MANE Select	ENSP00000390600.2:n.3088-90_3088-89insT
ENST00000643924.1:c.3088-93_3088-92insT	ENSP00000495595.1:n.3088-93_3088-92insT
ENST00000655275.1:c.3115-93_3115-92insT	ENSP00000499510.1:n.3115-93_3115-92insT
ENST00000449082.2:c.3088-90_3088-89insT	ENSP00000390600.2:n.3088-90_3088-89insT
NM_001293306.2:c.3088-93_3088-92insT	NP_001280235.2:n.3088-93_3088-92insT
NM_001293307.2:c.2794-90_2794-89insT	NP_001280236.2:n.2794-90_2794-89insT
NM_006514.3:c.3088-90_3088-89insT	NP_006505.3:n.3088-90_3088-89insT
XM_005265371.2:c.3097-90_3097-89insT	XP_005265428.1:n.3097-90_3097-89insT
XM_011533993.1:c.3097-93_3097-92insT	XP_011532295.1:n.3097-93_3097-92insT
XM_011533994.1:c.2803-90_2803-89insT	XP_011532296.1:n.2803-90_2803-89insT
XM_005265371.3:c.3097-90_3097-89insT	XP_005265428.1:n.3097-90_3097-89insT
XM_011533993.2:c.3097-93_3097-92insT	XP_011532295.1:n.3097-93_3097-92insT
XM_011533994.2:c.2803-90_2803-89insT	XP_011532296.1:n.2803-90_2803-89insT
NM_006514.4:c.3088-90_3088-89insT MANE Select	NP_006505.4:n.3088-90_3088-89insT