Canonical Allele Identifier: CA2577554073
Gene: SCN10A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.38725404del , CM000665.2:g.38725404del GRCh38
NC_000003.11:g.38766895del , CM000665.1:g.38766895del GRCh37
NC_000003.10:g.38741899del NCBI36
NG_031891.2:g.73608del

Transcript Alleles

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