Canonical Allele Identifier: CA1358778164

Gene: SCN11A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39032710_39032711delinsCA , CM000665.2:g.39032710_39032711delinsCA	GRCh38
NC_000003.11:g.39074201_39074202delinsCA , CM000665.1:g.39074201_39074202delinsCA	GRCh37
NC_000003.10:g.39049205_39049206delinsCA	NCBI36
NG_033859.2:g.24276_24277delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302328.9:c.-403-208_-403-207delinsTG MANE Select	ENSP00000307599.3:n.-403-208_-403-207delinsTG
ENST00000665106.1:n.82-208_82-207delinsTG
ENST00000668754.1:c.-903-208_-903-207delinsTG	ENSP00000499569.1:n.-903-208_-903-207delinsTG
ENST00000674755.1:n.233-208_233-207delinsTG
ENST00000675269.1:n.125-208_125-207delinsTG
ENST00000676333.1:n.39-208_39-207delinsTG
XM_011534335.1:c.49-208_49-207delinsTG	XP_011532637.1:n.49-208_49-207delinsTG
XM_011534336.1:c.49-208_49-207delinsTG	XP_011532638.1:n.49-208_49-207delinsTG
XR_940736.1:n.79-208_79-207delinsTG
XR_940737.1:n.79-208_79-207delinsTG
XR_940738.1:n.79-208_79-207delinsTG
XR_940739.1:n.79-208_79-207delinsTG
NM_001349253.1:c.-403-208_-403-207delinsTG	NP_001336182.1:n.-403-208_-403-207delinsTG
NM_001349253.2:c.-403-208_-403-207delinsTG MANE Select	NP_001336182.1:n.-403-208_-403-207delinsTG
NR_164473.1:n.85-208_85-207delinsTG