Canonical Allele Identifier: CA2810127638
Gene: SCN4A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63945645_63945646insGGAAAG , CM000679.2:g.63945645_63945646insGGAAAG GRCh38
NC_000017.10:g.62023005_62023006insGGAAAG , CM000679.1:g.62023005_62023006insGGAAAG GRCh37
NC_000017.9:g.59376737_59376738insGGAAAG NCBI36
NG_011699.1:g.32274_32275insTTTCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000435607.3:c.3442-7_3442-6insTTTCCC MANE Select ENSP00000396320.1:n.3442-7_3442-6insTTTCCC
ENST00000578147.5:c.3442-7_3442-6insTTTCCC ENSP00000463963.1:n.3442-7_3442-6insTTTCCC
NM_000334.4:c.3442-7_3442-6insTTTCCC MANE Select NP_000325.4:n.3442-7_3442-6insTTTCCC
XM_005257566.3:c.3442-7_3442-6insTTTCCC XP_005257623.1:n.3442-7_3442-6insTTTCCC