Canonical Allele Identifier: CA400633764
Gene: SCN4A HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.62038737T>A (hg19) chr17:g.63961377T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63961377T>A , CM000679.2:g.63961377T>A GRCh38
NC_000017.10:g.62038737T>A , CM000679.1:g.62038737T>A GRCh37
NC_000017.9:g.59392469T>A NCBI36
NG_011699.1:g.16542A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000435607.3:c.1661A>T MANE Select ENSP00000396320.1:p.Lys554Ile
ENST00000578147.5:c.1661A>T ENSP00000463963.1:p.Lys554Ile
ENST00000581514.1:n.317A>T
NM_000334.4:c.1661A>T MANE Select NP_000325.4:p.Lys554Ile
XM_005257566.3:c.1661A>T XP_005257623.1:p.Lys554Ile
XR_934910.1:n.124+655T>A
XR_001752969.1:n.1276+655T>A
XR_934910.2:n.1276+655T>A
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