Canonical Allele Identifier: CA2665099572
Gene: SCN10A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.38725185_38725186insAGTGGCGAATGCATCCTGTGGGGAGAGGGC , CM000665.2:g.38725185_38725186insAGTGGCGAATGCATCCTGTGGGGAGAGGGC GRCh38
NC_000003.11:g.38766676_38766677insAGTGGCGAATGCATCCTGTGGGGAGAGGGC , CM000665.1:g.38766676_38766677insAGTGGCGAATGCATCCTGTGGGGAGAGGGC GRCh37
NC_000003.10:g.38741680_38741681insAGTGGCGAATGCATCCTGTGGGGAGAGGGC NCBI36
NG_031891.2:g.73826_73827insCCCTCTCCCCACAGGATGCATTCGCCACTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000449082.3:c.3217_3218insCCCTCTCCCCACAGGATGCATTCGCCACTG MANE Select ENSP00000390600.2:p.Gln1072_Val1073insAlaLeuSerProGlnAspAlaPh...
ENST00000643924.1:c.3214_3215insCCCTCTCCCCACAGGATGCATTCGCCACTG ENSP00000495595.1:p.Gln1071_Val1072insAlaLeuSerProGlnAspAlaPh...
ENST00000655275.1:c.3241_3242insCCCTCTCCCCACAGGATGCATTCGCCACTG ENSP00000499510.1:p.Gln1080_Val1081insAlaLeuSerProGlnAspAlaPh...
ENST00000449082.2:c.3217_3218insCCCTCTCCCCACAGGATGCATTCGCCACTG ENSP00000390600.2:p.Gln1072_Val1073insAlaLeuSerProGlnAspAlaPh...
NM_001293306.2:c.3214_3215insCCCTCTCCCCACAGGATGCATTCGCCACTG NP_001280235.2:p.Gln1071_Val1072insAlaLeuSerProGlnAspAlaPheAl...
NM_001293307.2:c.2923_2924insCCCTCTCCCCACAGGATGCATTCGCCACTG NP_001280236.2:p.Gln974_Val975insAlaLeuSerProGlnAspAlaPheAlaT...
NM_006514.3:c.3217_3218insCCCTCTCCCCACAGGATGCATTCGCCACTG NP_006505.3:p.Gln1072_Val1073insAlaLeuSerProGlnAspAlaPheAlaTh...
XM_005265371.2:c.3226_3227insCCCTCTCCCCACAGGATGCATTCGCCACTG XP_005265428.1:p.Gln1075_Val1076insAlaLeuSerProGlnAspAlaPheAl...
XM_011533993.1:c.3223_3224insCCCTCTCCCCACAGGATGCATTCGCCACTG XP_011532295.1:p.Gln1074_Val1075insAlaLeuSerProGlnAspAlaPheAl...
XM_011533994.1:c.2932_2933insCCCTCTCCCCACAGGATGCATTCGCCACTG XP_011532296.1:p.Gln977_Val978insAlaLeuSerProGlnAspAlaPheAlaT...
XM_005265371.3:c.3226_3227insCCCTCTCCCCACAGGATGCATTCGCCACTG XP_005265428.1:p.Gln1075_Val1076insAlaLeuSerProGlnAspAlaPheAl...
XM_011533993.2:c.3223_3224insCCCTCTCCCCACAGGATGCATTCGCCACTG XP_011532295.1:p.Gln1074_Val1075insAlaLeuSerProGlnAspAlaPheAl...
XM_011533994.2:c.2932_2933insCCCTCTCCCCACAGGATGCATTCGCCACTG XP_011532296.1:p.Gln977_Val978insAlaLeuSerProGlnAspAlaPheAlaT...
NM_006514.4:c.3217_3218insCCCTCTCCCCACAGGATGCATTCGCCACTG MANE Select NP_006505.4:p.Gln1072_Val1073insAlaLeuSerProGlnAspAlaPheAlaTh...