Canonical Allele Identifier: CA1304927938
Gene: SCN9A HGNC NCBI
SCN1A-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1693241045

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.166196083T>G , CM000664.2:g.166196083T>G GRCh38
NC_000002.11:g.167052593T>G , CM000664.1:g.167052593T>G GRCh37
NC_000002.10:g.166760839T>G NCBI36
NG_012798.1:g.184905A>C , LRG_369:g.184905A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000303354.11:c.*2589A>C (SCN9A) ENSP00000304748.7:n.*2589A>C
ENST00000642356.2:c.*2589A>C (SCN9A) MANE Select ENSP00000495601.1:n.*2589A>C
ENST00000303354.10:c.*2589A>C (SCN9A) ENSP00000304748.7:n.*2589A>C
ENST00000409672.5:c.*2589A>C (SCN9A) ENSP00000386306.1:n.*2589A>C
NM_002977.3:c.*2589A>C , LRG_369t1:c.*2589A>C (SCN9A) NP_002968.1:n.*2589A>C
NR_110260.1:n.432-3556T>G (SCN1A-AS1)
NM_001365536.1:c.*2589A>C (SCN9A) MANE Select NP_001352465.1:n.*2589A>C