Canonical Allele Identifier: CA501349156
Gene: SCN4A HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.62038703C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63961343C>G , CM000679.2:g.63961343C>G GRCh38
NC_000017.10:g.62038703C>G , CM000679.1:g.62038703C>G GRCh37
NC_000017.9:g.59392435C>G NCBI36
NG_011699.1:g.16576G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000435607.3:c.1695G>C MANE Select ENSP00000396320.1:p.Leu565=
ENST00000578147.5:c.1695G>C ENSP00000463963.1:p.Leu565=
ENST00000581514.1:n.351G>C
NM_000334.4:c.1695G>C MANE Select NP_000325.4:p.Leu565=
XM_005257566.3:c.1695G>C XP_005257623.1:p.Leu565=
XR_934910.1:n.124+621C>G
XR_001752969.1:n.1276+621C>G
XR_934910.2:n.1276+621C>G
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