Canonical Allele Identifier: CA1358778033

Gene: SCN11A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39032588_39032589delinsAG , CM000665.2:g.39032588_39032589delinsAG	GRCh38
NC_000003.11:g.39074079_39074080delinsAG , CM000665.1:g.39074079_39074080delinsAG	GRCh37
NC_000003.10:g.39049083_39049084delinsAG	NCBI36
NG_033859.2:g.24398_24399delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302328.9:c.-403-86_-403-85delinsCT MANE Select	ENSP00000307599.3:n.-403-86_-403-85delinsCT
ENST00000665106.1:n.82-86_82-85delinsCT
ENST00000668754.1:c.-903-86_-903-85delinsCT	ENSP00000499569.1:n.-903-86_-903-85delinsCT
ENST00000674755.1:n.233-86_233-85delinsCT
ENST00000675269.1:n.125-86_125-85delinsCT
ENST00000676333.1:n.39-86_39-85delinsCT
XM_011534335.1:c.49-86_49-85delinsCT	XP_011532637.1:n.49-86_49-85delinsCT
XM_011534336.1:c.49-86_49-85delinsCT	XP_011532638.1:n.49-86_49-85delinsCT
XR_940736.1:n.79-86_79-85delinsCT
XR_940737.1:n.79-86_79-85delinsCT
XR_940738.1:n.79-86_79-85delinsCT
XR_940739.1:n.79-86_79-85delinsCT
NM_001349253.1:c.-403-86_-403-85delinsCT	NP_001336182.1:n.-403-86_-403-85delinsCT
NM_001349253.2:c.-403-86_-403-85delinsCT MANE Select	NP_001336182.1:n.-403-86_-403-85delinsCT
NR_164473.1:n.85-86_85-85delinsCT