Canonical Allele Identifier: CA10611612
Gene: SCN9A HGNC NCBI
SCN1A-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 331938
dbSNP Id: rs16851754

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.166197659G>A , CM000664.2:g.166197659G>A GRCh38
NC_000002.11:g.167054169G>A , CM000664.1:g.167054169G>A GRCh37
NC_000002.10:g.166762415G>A NCBI36
NG_012798.1:g.183329C>T , LRG_369:g.183329C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000303354.11:c.*1013C>T (SCN9A) ENSP00000304748.7:n.*1013C>T
ENST00000642356.2:c.*1013C>T (SCN9A) MANE Select ENSP00000495601.1:n.*1013C>T
ENST00000645907.1:c.*1013C>T (SCN9A) ENSP00000495983.1:n.*1013C>T
ENST00000303354.10:c.*1013C>T (SCN9A) ENSP00000304748.7:n.*1013C>T
ENST00000409672.5:c.*1013C>T (SCN9A) ENSP00000386306.1:n.*1013C>T
NM_002977.3:c.*1013C>T , LRG_369t1:c.*1013C>T (SCN9A) NP_002968.1:n.*1013C>T
NR_110260.1:n.432-1980G>A (SCN1A-AS1)
NM_001365536.1:c.*1013C>T (SCN9A) MANE Select NP_001352465.1:n.*1013C>T