Canonical Allele Identifier: CA2270170512

Gene: SCN4A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63961342T= , CM000679.2:g.63961342T=	GRCh38
NC_000017.10:g.62038702T= , CM000679.1:g.62038702T=	GRCh37
NC_000017.9:g.59392434T=	NCBI36
NG_011699.1:g.16577A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435607.3:c.1696A= MANE Select	ENSP00000396320.1:p.Lys566=
ENST00000578147.5:c.1696A=	ENSP00000463963.1:p.Lys566=
ENST00000581514.1:n.352A=
NM_000334.4:c.1696A= MANE Select	NP_000325.4:p.Lys566=
XM_005257566.3:c.1696A=	XP_005257623.1:p.Lys566=
XR_934910.1:n.124+620T=
XR_001752969.1:n.1276+620T=
XR_934910.2:n.1276+620T=