Canonical Allele Identifier: CA1358778204

Gene: SCN11A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39032774C= , CM000665.2:g.39032774C=	GRCh38
NC_000003.11:g.39074265C= , CM000665.1:g.39074265C=	GRCh37
NC_000003.10:g.39049269C=	NCBI36
NG_033859.2:g.24213G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302328.9:c.-403-271G= MANE Select	ENSP00000307599.3:n.-403-271G=
ENST00000665106.1:n.82-271G=
ENST00000668754.1:c.-903-271G=	ENSP00000499569.1:n.-903-271G=
ENST00000674755.1:n.233-271G=
ENST00000675269.1:n.125-271G=
ENST00000676333.1:n.39-271G=
XM_011534335.1:c.49-271G=	XP_011532637.1:n.49-271G=
XM_011534336.1:c.49-271G=	XP_011532638.1:n.49-271G=
XR_940736.1:n.79-271G=
XR_940737.1:n.79-271G=
XR_940738.1:n.79-271G=
XR_940739.1:n.79-271G=
NM_001349253.1:c.-403-271G=	NP_001336182.1:n.-403-271G=
NM_001349253.2:c.-403-271G= MANE Select	NP_001336182.1:n.-403-271G=
NR_164473.1:n.85-271G=