Canonical Allele Identifier: CA1358778089

Gene: SCN11A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39032644T= , CM000665.2:g.39032644T=	GRCh38
NC_000003.11:g.39074135T= , CM000665.1:g.39074135T=	GRCh37
NC_000003.10:g.39049139T=	NCBI36
NG_033859.2:g.24343A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302328.9:c.-403-141A= MANE Select	ENSP00000307599.3:n.-403-141A=
ENST00000665106.1:n.82-141A=
ENST00000668754.1:c.-903-141A=	ENSP00000499569.1:n.-903-141A=
ENST00000674755.1:n.233-141A=
ENST00000675269.1:n.125-141A=
ENST00000676333.1:n.39-141A=
XM_011534335.1:c.49-141A=	XP_011532637.1:n.49-141A=
XM_011534336.1:c.49-141A=	XP_011532638.1:n.49-141A=
XR_940736.1:n.79-141A=
XR_940737.1:n.79-141A=
XR_940738.1:n.79-141A=
XR_940739.1:n.79-141A=
NM_001349253.1:c.-403-141A=	NP_001336182.1:n.-403-141A=
NM_001349253.2:c.-403-141A= MANE Select	NP_001336182.1:n.-403-141A=
NR_164473.1:n.85-141A=