Canonical Allele Identifier: CA400616581
Gene: SCN4A HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.62020308T>A (hg19) chr17:g.63942948T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63942948T>A , CM000679.2:g.63942948T>A GRCh38
NC_000017.10:g.62020308T>A , CM000679.1:g.62020308T>A GRCh37
NC_000017.9:g.59374040T>A NCBI36
NG_011699.1:g.34971A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000435607.3:c.4166A>T MANE Select ENSP00000396320.1:p.Asn1389Ile
ENST00000578147.5:c.4166A>T ENSP00000463963.1:p.Asn1389Ile
NM_000334.4:c.4166A>T MANE Select NP_000325.4:p.Asn1389Ile
XM_005257566.3:c.4166A>T XP_005257623.1:p.Asn1389Ile
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