Canonical Allele Identifier: CA1304927732
Gene: SCN9A HGNC NCBI
SCN1A-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.166195623_166195627delinsCTAAG , CM000664.2:g.166195623_166195627delinsCTAAG GRCh38
NC_000002.11:g.167052133_167052137delinsCTAAG , CM000664.1:g.167052133_167052137delinsCTAAG GRCh37
NC_000002.10:g.166760379_166760383delinsCTAAG NCBI36
NG_012798.1:g.185361_185365delinsCTTAG , LRG_369:g.185361_185365delinsCTTAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000303354.11:c.*3045_*3049delinsCTTAG (SCN9A) ENSP00000304748.7:n.*3045_*3049delinsCTTAG
ENST00000642356.2:c.*3045_*3049delinsCTTAG (SCN9A) MANE Select ENSP00000495601.1:n.*3045_*3049delinsCTTAG
ENST00000303354.10:c.*3045_*3049delinsCTTAG (SCN9A) ENSP00000304748.7:n.*3045_*3049delinsCTTAG
ENST00000409672.5:c.*3045_*3049delinsCTTAG (SCN9A) ENSP00000386306.1:n.*3045_*3049delinsCTTAG
NM_002977.3:c.*3045_*3049delinsCTTAG , LRG_369t1:c.*3045_*3049delinsCTTAG (SCN9A) NP_002968.1:n.*3045_*3049delinsCTTAG
NR_110260.1:n.432-4016_432-4012delinsCTAAG (SCN1A-AS1)
NM_001365536.1:c.*3045_*3049delinsCTTAG (SCN9A) MANE Select NP_001352465.1:n.*3045_*3049delinsCTTAG