Canonical Allele Identifier: CA1358778038

Gene: SCN11A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39032595_39032597delinsCAG , CM000665.2:g.39032595_39032597delinsCAG	GRCh38
NC_000003.11:g.39074086_39074088delinsCAG , CM000665.1:g.39074086_39074088delinsCAG	GRCh37
NC_000003.10:g.39049090_39049092delinsCAG	NCBI36
NG_033859.2:g.24390_24392delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302328.9:c.-403-94_-403-92delinsCTG MANE Select	ENSP00000307599.3:n.-403-94_-403-92delinsCTG
ENST00000665106.1:n.82-94_82-92delinsCTG
ENST00000668754.1:c.-903-94_-903-92delinsCTG	ENSP00000499569.1:n.-903-94_-903-92delinsCTG
ENST00000674755.1:n.233-94_233-92delinsCTG
ENST00000675269.1:n.125-94_125-92delinsCTG
ENST00000676333.1:n.39-94_39-92delinsCTG
XM_011534335.1:c.49-94_49-92delinsCTG	XP_011532637.1:n.49-94_49-92delinsCTG
XM_011534336.1:c.49-94_49-92delinsCTG	XP_011532638.1:n.49-94_49-92delinsCTG
XR_940736.1:n.79-94_79-92delinsCTG
XR_940737.1:n.79-94_79-92delinsCTG
XR_940738.1:n.79-94_79-92delinsCTG
XR_940739.1:n.79-94_79-92delinsCTG
NM_001349253.1:c.-403-94_-403-92delinsCTG	NP_001336182.1:n.-403-94_-403-92delinsCTG
NM_001349253.2:c.-403-94_-403-92delinsCTG MANE Select	NP_001336182.1:n.-403-94_-403-92delinsCTG
NR_164473.1:n.85-94_85-92delinsCTG