Canonical Allele Identifier: CA2639310712
Gene: SCN4A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63971861_63971862insGAAAAAA , CM000679.2:g.63971861_63971862insGAAAAAA GRCh38
NC_000017.10:g.62049221_62049222insGAAAAAA , CM000679.1:g.62049221_62049222insGAAAAAA GRCh37
NC_000017.9:g.59402953_59402954insGAAAAAA NCBI36
NG_011699.1:g.6057_6058insTTTTTTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000435607.3:c.483-12_483-11insTTTTTTC MANE Select ENSP00000396320.1:n.483-12_483-11insTTTTTTC
ENST00000578147.5:c.483-12_483-11insTTTTTTC ENSP00000463963.1:n.483-12_483-11insTTTTTTC
NM_000334.4:c.483-12_483-11insTTTTTTC MANE Select NP_000325.4:n.483-12_483-11insTTTTTTC
XM_005257566.3:c.483-12_483-11insTTTTTTC XP_005257623.1:n.483-12_483-11insTTTTTTC