Canonical Allele Identifier: CA10611608
Gene: SCN9A HGNC NCBI
SCN1A-AS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.166197658C>T , CM000664.2:g.166197658C>T GRCh38
NC_000002.11:g.167054168C>T , CM000664.1:g.167054168C>T GRCh37
NC_000002.10:g.166762414C>T NCBI36
NG_012798.1:g.183330G>A , LRG_369:g.183330G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000303354.11:c.*1014G>A (SCN9A) ENSP00000304748.7:n.*1014G>A
ENST00000642356.2:c.*1014G>A (SCN9A) MANE Select ENSP00000495601.1:n.*1014G>A
ENST00000645907.1:c.*1014G>A (SCN9A) ENSP00000495983.1:n.*1014G>A
ENST00000303354.10:c.*1014G>A (SCN9A) ENSP00000304748.7:n.*1014G>A
ENST00000409672.5:c.*1014G>A (SCN9A) ENSP00000386306.1:n.*1014G>A
NM_002977.3:c.*1014G>A , LRG_369t1:c.*1014G>A (SCN9A) NP_002968.1:n.*1014G>A
NR_110260.1:n.432-1981C>T (SCN1A-AS1)
NM_001365536.1:c.*1014G>A (SCN9A) MANE Select NP_001352465.1:n.*1014G>A
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