Canonical Allele Identifier: CA2270170505

Gene: SCN4A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63961332T= , CM000679.2:g.63961332T=	GRCh38
NC_000017.10:g.62038692T= , CM000679.1:g.62038692T=	GRCh37
NC_000017.9:g.59392424T=	NCBI36
NG_011699.1:g.16587A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435607.3:c.1706A= MANE Select	ENSP00000396320.1:p.Asn569=
ENST00000578147.5:c.1706A=	ENSP00000463963.1:p.Asn569=
ENST00000581514.1:n.362A=
NM_000334.4:c.1706A= MANE Select	NP_000325.4:p.Asn569=
XM_005257566.3:c.1706A=	XP_005257623.1:p.Asn569=
XR_934910.1:n.124+610T=
XR_001752969.1:n.1276+610T=
XR_934910.2:n.1276+610T=