Canonical Allele Identifier: CA1304927932
Gene: SCN9A HGNC NCBI
SCN1A-AS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.166196059T= , CM000664.2:g.166196059T= GRCh38
NC_000002.11:g.167052569T= , CM000664.1:g.167052569T= GRCh37
NC_000002.10:g.166760815T= NCBI36
NG_012798.1:g.184929A= , LRG_369:g.184929A=

Transcript Alleles

HGVS Amino-acid change
ENST00000303354.11:c.*2613A= (SCN9A) ENSP00000304748.7:n.*2613A=
ENST00000642356.2:c.*2613A= (SCN9A) MANE Select ENSP00000495601.1:n.*2613A=
ENST00000303354.10:c.*2613A= (SCN9A) ENSP00000304748.7:n.*2613A=
ENST00000409672.5:c.*2613A= (SCN9A) ENSP00000386306.1:n.*2613A=
NM_002977.3:c.*2613A= , LRG_369t1:c.*2613A= (SCN9A) NP_002968.1:n.*2613A=
NR_110260.1:n.432-3580T= (SCN1A-AS1)
NM_001365536.1:c.*2613A= (SCN9A) MANE Select NP_001352465.1:n.*2613A=
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