Canonical Allele Identifier: CA2755909975

Gene: SCN11A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39032745T>A , CM000665.2:g.39032745T>A	GRCh38
NC_000003.11:g.39074236T>A , CM000665.1:g.39074236T>A	GRCh37
NC_000003.10:g.39049240T>A	NCBI36
NG_033859.2:g.24242A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302328.9:c.-403-242A>T MANE Select	ENSP00000307599.3:n.-403-242A>T
ENST00000665106.1:n.82-242A>T
ENST00000668754.1:c.-903-242A>T	ENSP00000499569.1:n.-903-242A>T
ENST00000674755.1:n.233-242A>T
ENST00000675269.1:n.125-242A>T
ENST00000676333.1:n.39-242A>T
XM_011534335.1:c.49-242A>T	XP_011532637.1:n.49-242A>T
XM_011534336.1:c.49-242A>T	XP_011532638.1:n.49-242A>T
XR_940736.1:n.79-242A>T
XR_940737.1:n.79-242A>T
XR_940738.1:n.79-242A>T
XR_940739.1:n.79-242A>T
NM_001349253.1:c.-403-242A>T	NP_001336182.1:n.-403-242A>T
NM_001349253.2:c.-403-242A>T MANE Select	NP_001336182.1:n.-403-242A>T
NR_164473.1:n.85-242A>T