Canonical Allele Identifier: CA8710025
Gene: SCN4A HGNC NCBI

Linked Data

dbSNP Id: rs772788036

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63968221_63968222del , CM000679.2:g.63968221_63968222del GRCh38
NC_000017.10:g.62045581_62045582del , CM000679.1:g.62045581_62045582del GRCh37
NC_000017.9:g.59399313_59399314del NCBI36
NG_011699.1:g.9702_9703del

Transcript Alleles

HGVS Amino-acid Change
ENST00000435607.3:c.842_843del MANE Select ENSP00000396320.1:p.Val281AlafsTer17
ENST00000578147.5:c.842_843del ENSP00000463963.1:p.Val281AlafsTer17
NM_000334.4:c.842_843del MANE Select NP_000325.4:p.Val281AlafsTer17
XM_005257566.3:c.842_843del XP_005257623.1:p.Val281AlafsTer17