Canonical Allele Identifier: CA2270160899
Gene: SCN4A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63941357T= , CM000679.2:g.63941357T= GRCh38
NC_000017.10:g.62018717T= , CM000679.1:g.62018717T= GRCh37
NC_000017.9:g.59372449T= NCBI36
NG_011699.1:g.36562A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000435607.3:c.4925A= MANE Select ENSP00000396320.1:p.Asp1642=
ENST00000578147.5:c.4925A= ENSP00000463963.1:p.Asp1642=
NM_000334.4:c.4925A= MANE Select NP_000325.4:p.Asp1642=
XM_005257566.3:c.4925A= XP_005257623.1:p.Asp1642=
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