Canonical Allele Identifier: CA400616585
Gene: SCN4A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63942949T>G , CM000679.2:g.63942949T>G GRCh38
NC_000017.10:g.62020309T>G , CM000679.1:g.62020309T>G GRCh37
NC_000017.9:g.59374041T>G NCBI36
NG_011699.1:g.34970A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000435607.3:c.4165A>C MANE Select ENSP00000396320.1:p.Asn1389His
ENST00000578147.5:c.4165A>C ENSP00000463963.1:p.Asn1389His
NM_000334.4:c.4165A>C MANE Select NP_000325.4:p.Asn1389His
XM_005257566.3:c.4165A>C XP_005257623.1:p.Asn1389His