Canonical Allele Identifier: CA2270161362
Gene: SCN4A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63942260_63942273delinsTGTGTGTGTGTGTG , CM000679.2:g.63942260_63942273delinsTGTGTGTGTGTGTG GRCh38
NC_000017.10:g.62019620_62019633delinsTGTGTGTGTGTGTG , CM000679.1:g.62019620_62019633delinsTGTGTGTGTGTGTG GRCh37
NC_000017.9:g.59373352_59373365delinsTGTGTGTGTGTGTG NCBI36
NG_011699.1:g.35646_35659delinsCACACACACACACA

Transcript Alleles

HGVS Amino-acid Change
ENST00000435607.3:c.4289-280_4289-267delinsCACACACACACACA MANE Select ENSP00000396320.1:n.4289-280_4289-267delinsCACACACACACACA
ENST00000578147.5:c.4289-280_4289-267delinsCACACACACACACA ENSP00000463963.1:n.4289-280_4289-267delinsCACACACACACACA
NM_000334.4:c.4289-280_4289-267delinsCACACACACACACA MANE Select NP_000325.4:n.4289-280_4289-267delinsCACACACACACACA
XM_005257566.3:c.4289-280_4289-267delinsCACACACACACACA XP_005257623.1:n.4289-280_4289-267delinsCACACACACACACA