Canonical Allele Identifier: CA2665100330
Gene: SCN10A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.38725411_38725412del , CM000665.2:g.38725411_38725412del GRCh38
NC_000003.11:g.38766902_38766903del , CM000665.1:g.38766902_38766903del GRCh37
NC_000003.10:g.38741906_38741907del NCBI36
NG_031891.2:g.73599_73600del

Transcript Alleles

HGVS Amino-acid Change
ENST00000449082.3:c.3088-98_3088-97del MANE Select ENSP00000390600.2:n.3088-98_3088-97del
ENST00000643924.1:c.3088-101_3088-100del ENSP00000495595.1:n.3088-101_3088-100del
ENST00000655275.1:c.3115-101_3115-100del ENSP00000499510.1:n.3115-101_3115-100del
ENST00000449082.2:c.3088-98_3088-97del ENSP00000390600.2:n.3088-98_3088-97del
NM_001293306.2:c.3088-101_3088-100del NP_001280235.2:n.3088-101_3088-100del
NM_001293307.2:c.2794-98_2794-97del NP_001280236.2:n.2794-98_2794-97del
NM_006514.3:c.3088-98_3088-97del NP_006505.3:n.3088-98_3088-97del
XM_005265371.2:c.3097-98_3097-97del XP_005265428.1:n.3097-98_3097-97del
XM_011533993.1:c.3097-101_3097-100del XP_011532295.1:n.3097-101_3097-100del
XM_011533994.1:c.2803-98_2803-97del XP_011532296.1:n.2803-98_2803-97del
XM_005265371.3:c.3097-98_3097-97del XP_005265428.1:n.3097-98_3097-97del
XM_011533993.2:c.3097-101_3097-100del XP_011532295.1:n.3097-101_3097-100del
XM_011533994.2:c.2803-98_2803-97del XP_011532296.1:n.2803-98_2803-97del
NM_006514.4:c.3088-98_3088-97del MANE Select NP_006505.4:n.3088-98_3088-97del