Canonical Allele Identifier: CA2665100070

Gene: SCN10A

Linked Data

• gnomAD v4: 3-38725354-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38725356del , CM000665.2:g.38725356del	GRCh38
NC_000003.11:g.38766847del , CM000665.1:g.38766847del	GRCh37
NC_000003.10:g.38741851del	NCBI36
NG_031891.2:g.73656del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449082.3:c.3088-41del MANE Select	ENSP00000390600.2:n.3088-41del
ENST00000643924.1:c.3088-44del	ENSP00000495595.1:n.3088-44del
ENST00000655275.1:c.3115-44del	ENSP00000499510.1:n.3115-44del
ENST00000449082.2:c.3088-41del	ENSP00000390600.2:n.3088-41del
NM_001293306.2:c.3088-44del	NP_001280235.2:n.3088-44del
NM_001293307.2:c.2794-41del	NP_001280236.2:n.2794-41del
NM_006514.3:c.3088-41del	NP_006505.3:n.3088-41del
XM_005265371.2:c.3097-41del	XP_005265428.1:n.3097-41del
XM_011533993.1:c.3097-44del	XP_011532295.1:n.3097-44del
XM_011533994.1:c.2803-41del	XP_011532296.1:n.2803-41del
XM_005265371.3:c.3097-41del	XP_005265428.1:n.3097-41del
XM_011533993.2:c.3097-44del	XP_011532295.1:n.3097-44del
XM_011533994.2:c.2803-41del	XP_011532296.1:n.2803-41del
NM_006514.4:c.3088-41del MANE Select	NP_006505.4:n.3088-41del