Canonical Allele Identifier: CA1304927908
Gene: SCN9A HGNC NCBI
SCN1A-AS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.166196025G= , CM000664.2:g.166196025G= GRCh38
NC_000002.11:g.167052535G= , CM000664.1:g.167052535G= GRCh37
NC_000002.10:g.166760781G= NCBI36
NG_012798.1:g.184963C= , LRG_369:g.184963C=

Transcript Alleles

HGVS Amino-acid change
ENST00000303354.11:c.*2647C= (SCN9A) ENSP00000304748.7:n.*2647C=
ENST00000642356.2:c.*2647C= (SCN9A) MANE Select ENSP00000495601.1:n.*2647C=
ENST00000303354.10:c.*2647C= (SCN9A) ENSP00000304748.7:n.*2647C=
ENST00000409672.5:c.*2647C= (SCN9A) ENSP00000386306.1:n.*2647C=
NM_002977.3:c.*2647C= , LRG_369t1:c.*2647C= (SCN9A) NP_002968.1:n.*2647C=
NR_110260.1:n.432-3614G= (SCN1A-AS1)
NM_001365536.1:c.*2647C= (SCN9A) MANE Select NP_001352465.1:n.*2647C=
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