Canonical Allele Identifier: CA400633676

Gene: SCN4A

Linked Data

• MyVariant Identifiers: chr17:g.62038725C>T (hg19) ; chr17:g.63961365C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63961365C>T , CM000679.2:g.63961365C>T	GRCh38
NC_000017.10:g.62038725C>T , CM000679.1:g.62038725C>T	GRCh37
NC_000017.9:g.59392457C>T	NCBI36
NG_011699.1:g.16554G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435607.3:c.1673G>A MANE Select	ENSP00000396320.1:p.Trp558Ter
ENST00000578147.5:c.1673G>A	ENSP00000463963.1:p.Trp558Ter
ENST00000581514.1:n.329G>A
NM_000334.4:c.1673G>A MANE Select	NP_000325.4:p.Trp558Ter
XM_005257566.3:c.1673G>A	XP_005257623.1:p.Trp558Ter
XR_934910.1:n.124+643C>T
XR_001752969.1:n.1276+643C>T
XR_934910.2:n.1276+643C>T