Canonical Allele Identifier: CA2270160725
Gene: SCN4A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63941020_63941025delinsGTACAT , CM000679.2:g.63941020_63941025delinsGTACAT GRCh38
NC_000017.10:g.62018380_62018385delinsGTACAT , CM000679.1:g.62018380_62018385delinsGTACAT GRCh37
NC_000017.9:g.59372112_59372117delinsGTACAT NCBI36
NG_011699.1:g.36894_36899delinsATGTAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000435607.3:c.5257_5262delinsATGTAC MANE Select ENSP00000396320.1:p.Met1753=
ENST00000578147.5:c.5257_5262delinsATGTAC ENSP00000463963.1:p.Met1753=
NM_000334.4:c.5257_5262delinsATGTAC MANE Select NP_000325.4:p.Met1753=
XM_005257566.3:c.5257_5262delinsATGTAC XP_005257623.1:p.Met1753=