Canonical Allele Identifier: CA2270160766
Gene: SCN4A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63941085T= , CM000679.2:g.63941085T= GRCh38
NC_000017.10:g.62018445T= , CM000679.1:g.62018445T= GRCh37
NC_000017.9:g.59372177T= NCBI36
NG_011699.1:g.36834A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000435607.3:c.5197A= MANE Select ENSP00000396320.1:p.Lys1733=
ENST00000578147.5:c.5197A= ENSP00000463963.1:p.Lys1733=
NM_000334.4:c.5197A= MANE Select NP_000325.4:p.Lys1733=
XM_005257566.3:c.5197A= XP_005257623.1:p.Lys1733=
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